Suppression of cytokine release syndrome in chimeric antigen receptor cell therapy

ABSTRACT

Disclosed herein are methods of gene editing, or endogenous suppression, of cytokines/chemokines/transcription factors secreted from chimeric antigen receptor (CAR)-bearing immune effector cell such as CAR-T cells for the mitigation of cytokine release syndrome and/or CAR-T associated neuropathy. These methods involve insertion of the CAR into a locus of a cytokine gene, blocking its expression. Also disclosed herein are (CAR)-bearing immune effector cells with CARs inserted into a locus of a cytokine gene, and methods of treatment of diseases with immunotherapy with a reduced incidence of cytokine release syndrome and/or CAR-T associated neuropathy.

This application claims the benefit of U.S. Provisional Application No. 62/679,597, filed Jun. 1, 2018, the disclosure of which is hereby incorporated by reference in its entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Aug. 6, 2019, is named WGN0003-401-PC_SL.txt and is 956,834 bytes in size.

CAR-T cells have emerged as a promising therapy for the treatment of hematological malignancies. Despite remarkable clinical efficacy against B cell malignancies, the success of CAR-T therapy has been limited by severe, life-threatening toxicities, observed in over 50% of patients. These toxicities have resulted in several deaths leading to early termination of clinical trial. Toxicities primarily manifest as cytokine release syndrome (CRS, also referred to as “cytokine storm”) characterized by high elevations of cytokines including INFγ, granulocyte-macrophage colony-stimulating factor, IL-10, and IL-6. These cytokine elevations result in a plethora of clinical symptoms including fever, hypotension, organ dysfunction, respiratory failure and coagulopathy. CRS can be fatal. Additionally, neurotoxicity often presents even after the initial symptoms of CRS have subsided. The pathogenesis of CRS and associated neurotoxicity is poorly understood and further understanding of the mechanism would be useful for the successful translation of CAR-T therapy. In the meanwhile, disrupting the pathogenesis of CRS by reducing the level of cytokine genes available for expression is one way to mitigate the condition.

Disclosed herein are methods of gene deletion and endogenous suppression, of cytokines/chemokines/transcription factors secreted from chimeric antigen receptor (CAR)-bearing immune effector cell, such as CAR-T cell, for the mitigation of cytokine release syndrome and/or CAR-T associated neuropathy. These gene deletion methods may include, but are not limited to, insertion of the CAR into a locus of a cytokine/chemokine/transcription factor gene, blocking its expression; gene editing with Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), or CRISPR; expression of an scFv with an endoplasmic reticulum (ER) binding tether to bind the cytokine in the ER and prevent secretion; and transfection of small hairpin RNAs (shRNAs) or small interfering RNAs (siRNAs). Also disclosed herein are CAR-bearing immune effector cells modified with these described cytokine/chemokine/transcription factor gene deletion methods, and methods of treatment of diseases with immunotherapy with a reduced incidence of cytokine release syndrome (CRS) and/or CAR-T associated neuropathy (CAN).

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 —Illustrates the concept of inserting a CAR into the gene for a cytokine in order to block its translation, thereby deleting it or reducing its level, thus preventing or reducing cytokine release syndrome and/or CAR-bearing immune effector cell associated neuropathy (CAR-T associated neuropathy).

FIG. 2 —Shows a timeline for a method of treatment of hematologic malignancies using the CAR-T cells disclosed herein. Those of skill in the art will appreciate that some flexibility is possible in the time frames shown.

FIG. 3 —Shows the AAV donor construct for insertion of CD34 into the GM-CSF locus.

FIG. 4 —Shows the WC40 plasmid vector for use in inserting GFP into the CD38 locus.

FIG. 5 —Shows the AAV donor construct for insertion of GFP into the CD38 locus.

FIG. 6 —Shows a CAR19-GM-CSF PEBL-trCD34 construct.

FIG. 7 —Shows IL-6 expression in T cells, iDC cells, T cells+iDC, T cells+beads, and iDC+beads+ T cells for GM-CSF knock-out, wild-type, and controls at 24 hours.

FIG. 8 —Shows IL-6 expression in CAR19, iDC only, Act MQ only, MC only, RAMOS only, CAR19+iDC, CAR19+ActMQ, CAR19+MQ, CAR19+RAMOS, iDC+RAMOS+CAR-T, ActMQ+RAMOS+CAR-T, and MQ+RAMOS+CAR-T for CAR19 GM-CSF knock-out, CAR19, and controls at 24 hours.

FIG. 9 —Shows IL-6 expression in T cells, iDC cells, T cells+iDC, T cells+beads, and iDC+beads+ T cells for GM-CSF knock-out, wild-type, and controls at 48 hours.

FIG. 10 —Shows IL-6 expression in CAR19, iDC only, Act MQ only, MC only, RAMOS only, CAR19+iDC, CAR19+ActMQ, CAR19+MQ, CAR19+RAMOS, iDC+RAMOS+CAR-T, ActMQ+RAMOS+CAR-T, and MQ+RAMOS+CAR-T for CAR19 GM-CSF knock-out, CAR19, and controls at 48 hours.

FIG. 11 —Shows a set-up of an ELISA plate for detecting specific markers of CAR-T cells.

FIG. 12 a and FIG. 12 b —Shows the results for an ELISA assay detecting specific markers of the CAR-T cells. FIG. 12 a shows the top half of the ELISA plate, and FIG. 12 b shows the bottom half of the plate. In each of rows A-H, from top to bottom, the sub-rows indicate [450] test, [540] ref, Pathlength, 450, 540, Corrected [450], and Corrected [540].

DETAILED DESCRIPTION

Accordingly, disclosed herein as Embodiment 1 is a chimeric antigen receptor (CAR)-bearing immune effector cell that is deficient in a cytokine or in a chemokine or in a transcription factor that is involved in cytokine release syndrome.

The following disclosure will detail embodiments, alternatives, and uses of the cytokine-deficient cells, as well as the use of such cells in, for example, immunotherapy and adoptive cell transfer for the treatment of diseases. Accordingly, provided herein are the following additional embodiments.

Embodiment 2—The cell as recited in embodiment 1, wherein the cytokine or chemokine or transcription factor deficiency is effected by deletion or suppression of a gene encoding the cytokine or chemokine or transcription factor.

Embodiment 3—The cell as recited in any of embodiments 1 or 2, wherein the deletion or suppression is effected by inserting the CAR into a locus of the cytokine or chemokine or transcription factor gene.

Embodiment 4—The cell as recited in any of embodiments 1 to 3, wherein the CAR is part of a construct that also includes a selectable marker.

Embodiment 5—The cell as recited in any of embodiments 1 to 4, wherein the selectable marker comprises a green fluorescence (GFP) gene, a yellow fluorescent (YFP) gene, a truncated CD34 (tCD34) gene, or a truncated EGFR (tEGFR) gene.

Embodiment 6—The cell as recited in any of embodiments 1 to 5, wherein the cytokine or chemokine or transcription factor deficiency is effected by deletion or suppression of the cytokine or chemokine gene, by Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), or Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) editing.

Embodiment 7—The cell as recited in any of embodiments 1 to 6, wherein deletion or suppression is effected using CRISPR.

Embodiment 8—The cell as recited in any of embodiments 1 to 7, wherein deletion or suppression is effected using Cas9-CRISPR.

Embodiment 9—The cell as recited in any of embodiments 1 to 8, wherein the Cas9 is delivered into the cell as mRNA or protein.

Embodiment 10—The cell as recited in any of embodiments 1 to 9, wherein the Cas9 is delivered into the cell as mRNA.

Embodiment 11—The cell as recited in any of embodiments 1 to 10, wherein the Cas9 is delivered into the cell as protein.

Embodiment 12—The cell as recited in any of embodiments 1 to 11, wherein a guide RNA (gRNA) targeting the gene to be deleted or suppressed is delivered contemporaneously with the Cas9.

Embodiment 13—The cell as recited in any of embodiments 1 to 12, wherein the delivery is by electroporation.

Embodiment 14—The cell as recited in any of embodiments 1 to 13, wherein the cytokine or chemokine or transcription factor deficiency is effected by suppression of the cytokine or chemokine or transcription factor gene transcript by transfection of one or more types of small interfering RNAs (siRNA).

Embodiment 15—The cell as recited in any of embodiments 1 to 14, wherein the cytokine or chemokine or transcription factor deficiency is effected by suppression of the cytokine or chemokine or transcription factor gene transcript by transduction of one or more types of short hairpin RNAs (shRNA).

Embodiment 16—A chimeric antigen receptor (CAR)-bearing immune effector cell expressing at least one CAR, wherein:

the at least one CAR is inserted into a locus of a cytokine or chemokine or transcription factor gene or transcription factor gene;

the cytokine or chemokine or transcription factor gene is deleted or suppressed by a method chosen from Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), and Clustered Regularly Interspaces Short Palindromic Repeats (CRISPR) editing;

the cytokine or chemokine or transcription factor is suppressed by expression of an scFv with an endoplasmic reticulum (ER) binding tether to bind the cytokine or chemokine in the ER and prevent secretion;

the cytokine or chemokine or transcription factor gene transcript is suppressed by transfection of small interfering RNAs (siRNAs); or

the cytokine or chemokine or transcription factor gene transcript is suppressed by transduction of short hairpin RNAs (shRNAs).

Embodiment 17—The cell as recited in any of embodiments 1 to 16, wherein the cell is chosen from a chimeric antigen receptor T cell (CAR-T), a CAR-bearing iNKT cell (iNKT-CAR), and a CAR-bearing natural killer (NK) cell (NK-CAR), or a CAR-bearing macrophage.

Embodiment 18—The cell as recited in any of embodiments 1 to 17, wherein the cell is a CAR-T.

Embodiment 19—The cell as recited in any of embodiments 1 to 18, wherein the cell is a dual or tandem CAR-T.

Embodiment 20—The cell as recited in any of embodiments 1 to 17, wherein the cell is an iNKT-CAR.

Embodiment 21—The cell as recited in any of embodiments 1 to 20, wherein the cell is a dual or tandem iNKT-CAR.

Embodiment 22—The cell as recited in any of embodiments 1 to 17, wherein the cell is a CAR-macrophage.

Embodiment 23—The cell as recited in any of embodiments 1 to 22, wherein the cell is a dual or tandem CAR-macrophage.

Embodiment 24—The cell as recited in any of embodiments 1 to 23, wherein the cytokine or chemokine or transcription factor contributes to the development of cytokine release syndrome.

Embodiment 25—The cell as recited in any of embodiments 1 to 24, wherein the cytokine or chemokine or transcription factor is selected from among those recited in Table 10.

Embodiment 26—The cell as recited in any of embodiments 1 to 25, wherein the cytokine or chemokine or transcription factor is produced by T cells that activate or localize myeloid cells.

Embodiment 27—The cell as recited in any of embodiments 1 to 26, wherein the cytokine or chemokine or transcription factor is a T cell surface receptor gene that activates myeloid or CAR-T cells.

Embodiment 28—The cell as recited in any of embodiments 1 to 27, wherein the gene that is deleted or suppressed is a T cell surface receptor that is integrated into CAR-T cell signaling.

Embodiment 29—The cell as recited in any of embodiments 1 to 28, wherein the cytokine or chemokine or transcription factor drives T cell/CAR-T cell differentiation.

Embodiment 30—The cell as recited in any of embodiments 1 to 29, wherein the cytokine or chemokine is a transcription factor that drives T cell/CAR-T cell differentiation.

Embodiment 31—The cell as recited in any of embodiments 1 to 30, wherein the cytokine or chemokine or transcription factor is chosen from MCP1 (CCL2), MCP-2, GM-CSF, G-CSF, M-CSF, Il-4, and IFNγ.

Embodiment 32—The cell as recited in any of embodiments 1 to 31, wherein the cytokine or chemokine or transcription factor is GM-CSF.

Embodiment 33—The cell as recited in any of embodiments 1 to 32, wherein the cell is a GM-CSF deficient CAR-T cell.

Embodiment 34—The cell as recited in any of embodiments 1 to 33, wherein the cell is a GM-CSF deficient iNKT-CAR cell.

Embodiment 35—The cell as recited in any of embodiments 1 to 34, wherein the immune effector cells to be used are harvested from a healthy donor.

Embodiment 36—The cell as recited in any of embodiments 1 to 35, wherein the donor is a human.

Embodiment 37—The cell as recited in any of embodiments 1 to 36, wherein the chimeric antigen receptor(s) specifically binds at least one antigen expressed on a malignant cell.

Embodiment 38—The cell as recited in any of embodiments 1 to 37, wherein the one or more antigens expressed on a malignant cell is chosen from BCMA, CS1, CD38, CD138, CD19, CD33, CD123, CD371, CD117, CD135, Tim-3, CD5, CD7, CD2, CD4, CD3, CD79A, CD79B, APRIL, CD56, and CD1a.

Embodiment 39—The cell as recited in any of embodiments 1 to 38, wherein the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant T cell.

Embodiment 40—The cell as recited in any of embodiments 1 to 39, wherein the antigen is selected from CD2, CD38, CD4, CD5, CD7, TCRA, and TCRβ.

Embodiment 41—The cell as recited in any of embodiments 1 to 38, wherein the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant B cell.

Embodiment 42—The cell as recited in any of embodiments 1 to 41, wherein the antigen is selected from CD19, CD20, CD21, CD22, CD23, CD24, CD25, CD27, CD38, and CD45.

Embodiment 43—The cell as recited in any of embodiments 1 to 42, wherein the antigen is selected from CD19 and CD20.

Embodiment 44—The cell as recited in any of embodiments 1 to 38, wherein the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant mesothelial cell.

Embodiment 45—The cell as recited in any of embodiments 1 to 44, wherein the antigen is mesothelin.

Embodiment 46—The cell as recited in any of embodiments 1 to 38, wherein the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant plasma cell.

Embodiment 47—The cell as recited in any of embodiments 1 to 46, wherein the antigen is selected from BCMA, CS1, CD38, and CD19.

Embodiment 48—The cell as recited in any of embodiments 1 to 47, wherein the chimeric antigen receptor expresses the extracellular portion of the APRIL protein, the ligand for BCMA and TACI, effectively co-targeting both BCMA and TACI.

Embodiment 49—The cell as recited in any of embodiments 1 to 48, wherein the CAR-T cell further comprises a suicide gene.

Embodiment 50—The cell as recited in any of embodiments 1 to 49, wherein endogenous T cell receptor mediated signaling is negligible in the cell.

Embodiment 51—The cell as recited in any of embodiments 1 to 50, wherein the cell does not induce alloreactivity or graft-versus-host disease.

Embodiment 52—The cell as recited in any of embodiments 1 to 51, wherein the cell does not induce fratricide.

Embodiment 53—A method of treatment of cancer in a patient, which has a reduced incidence of cytokine release syndrome and/or CAR-T associated neuropathy, comprising the administration of cells as recited in any of embodiments 1 to 52.

Embodiment 54—The method as recited in embodiment 53, wherein the cancer is a hematologic malignancy.

Embodiment 55—The method as recited in any of embodiments 53 to 54, wherein the hematologic malignancy is a T-cell malignancy.

Embodiment 56—The method as recited in any of embodiments 53 to 55, wherein the T cell malignancy is T-cell acute lymphoblastic leukemia (T-ALL).

Embodiment 57—The method as recited in any of embodiments 53 to 56, wherein the T cell malignancy is non-Hodgkin's lymphoma.

Embodiment 58—The method as recited in any of embodiments 53 to 57, wherein the hematologic malignancy is multiple myeloma.

Embodiment 59—The method as recited in any of embodiments 53 to 58, wherein the hematologic malignancy is AML.

Embodiment 60—The method as recited in any of embodiments 53 to 59, wherein the cancer is a solid tumor.

Embodiment 61—The method as recited any of embodiments 53 to 60, wherein the cancer is cervical cancer, pancreatic cancer, ovarian cancer, mesothelioma, and lung cancer.

Embodiment 62—A method of prevention or reduction of cytokine release syndrome or CAR-T associated neuropathy in a patient receiving chimeric antigen receptor T cell (CAR-T), CAR-bearing iNKT cell (iNKT-CAR), CAR-bearing natural killer (NK) cell (NK-CAR), or CAR-bearing macrophage (CAR-macrophage) immunotherapy, comprising the administration of cells as recited in any of embodiments 53 to 61 as the immunotherapy.

Embodiment 63—The method of any of embodiments 53 to 62, wherein the patient is being treated for cancer.

Embodiment 64—The method as recited in any of embodiments 53 to 63, wherein the cancer is a hematologic malignancy.

Embodiment 65—The method as recited in any of embodiments 53 to 64, wherein the hematologic malignancy is a T-cell malignancy.

Embodiment 66—The method as recited in any of embodiments 53 to 65, wherein the T cell malignancy is T-cell acute lymphoblastic leukemia (T-ALL).

Embodiment 67—The method as recited in any of embodiments 53 to 66, wherein the T cell malignancy is non-Hodgkin's lymphoma.

Embodiment 68—The method as recited in any of embodiments 53 to 67, wherein the hematologic malignancy is multiple myeloma.

Embodiment 69—The method as recited in any of embodiments 53 to 68, wherein the hematologic malignancy is AML.

Embodiment 70—The method as recited in any of embodiments 53 to 69, wherein the cancer is a solid tumor.

Embodiment 71—The method as recited in any of embodiments 53 to 70, wherein the cancer is cervical cancer, pancreatic cancer, ovarian cancer, mesothelioma, and lung cancer.

Embodiment 72—A method of blocking the expression of a cytokine gene or chemokine gene or transcription factor gene in a chimeric antigen receptor T cell (CAR-T), CAR-bearing iNKT cell (iNKT-CAR), CAR-bearing natural killer (NK) cell (NK-CAR), or CAR-bearing macrophage (CAR-macrophage) comprising the insertion of a CAR into a locus of the cytokine gene or chemokine gene or transcription factor gene.

Embodiment 73—The method of any of embodiments 53 to 72, wherein blocking the expression of the cytokine gene or chemokine gene or transcription factor gene does not reduce CAR-T cell-mediated killing.

Embodiment 74—A method of making a CAR-T (immune effector) cell that does not cause or contribute to CRS or CAR-T-associated neuropathy (CAN) comprising deleting or suppressing a cytokine or chemokine or transcription factor gene.

Embodiment 75—The method of any of embodiments 53 to 74, wherein deleting or suppressing the cytokine or chemokine or transcription factor gene does not reduce CAR-T cell-mediated killing.

Embodiment 76—The method as recited in any of embodiments 53 to 75, wherein the deletion or suppression is effected by inserting the CAR into a locus of the cytokine or chemokine or transcription factor gene.

Embodiment 77—The method as recited in any of embodiments 53 to 76, wherein the CAR is part of a construct that also includes a selectable marker.

Embodiment 78—The method as recited in any of embodiments 53 to 77, wherein the selectable marker comprises a green fluorescence (GFP) gene, a YFP gene, a tCD34 gene, or a tEGFR gene.

Embodiment 79—The method of any of embodiments 53 to 78, wherein the insertion of a CAR with a selectable marker into the cytokine or chemokine or transcription factor gene allows a single-step purification of TCR-negative cells.

Embodiment 80—The method of any of embodiments 53 to 79, wherein the insertion of a CAR with a selectable marker into the cytokine or chemokine or transcription factor gene allows a single step purification of CAR+ cytokine negative cells.

Embodiment 81—The method as recited in any of embodiments 53 to 80, wherein the deletion or suppression is effected using Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), or Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) editing.

Embodiment 82—The method as recited in any of embodiments 53 to 81, wherein the deletion or suppression is effected using CRISPR.

Embodiment 83—The method as recited in any of embodiments 53 to 82, wherein the deletion or suppression is effected using Cas9-CRISPR.

Embodiment 84—The method as recited in any of embodiments 53 to 83, wherein the Cas9 is delivered into the cell as mRNA or protein.

Embodiment 85—The method as recited in any of embodiments 53 to 84, wherein the Cas9 is delivered into the cell as mRNA.

Embodiment 86—The method as recited in any of embodiments 53 to 85, wherein the Cas9 is delivered into the cell as protein.

Embodiment 87—The method as recited in any of embodiments 53 to 86, wherein a guide RNA (gRNA) targeting the gene to be deleted or suppressed is delivered contemporaneously with the Cas9.

Embodiment 88—The method as recited in any of embodiments 53 to 87, wherein the delivery is by electroporation.

Embodiment 89—The method as recited in any of embodiments 53 to 88, wherein the deletion or suppression is effected by suppression of the cytokine or chemokine or transcription factor gene transcript by transduction of one or more types of short hairpin RNAs (shRNA).

Embodiment 90—The method as recited in any of embodiments 531 to 89, wherein the deletion or suppression is effected by transducing a construct encoding a protein expression blocker (PEBL).

Embodiment 91—The method of any of embodiments 53 to 90, wherein the construct encodes an antibody-derived single-chain variable fragment specific for the cytokine, chemokine or TF gene.

Embodiment 92—The method of any of embodiments 53 to 91, wherein deletion of the cytokine, chemokine, or transcription factor gene does not reduce CAR-T-mediated killing.

Embodiment 93—The method of any of embodiments 53 to 92, wherein the CAR to be inserted comprises a donor template.

Embodiment 94—The method of any of embodiments 53 to 93, wherein donor template comprises an adeno-associated virus (AAV), a single-stranded DNA, or a double-stranded DNA.

Disclosed herein is a chimeric antigen receptor (CAR)-bearing immune effector cell that is deficient in a cytokine.

In certain embodiments, the cytokine deficiency is effected by ablation of a cytokine gene or a chemokine gene, or a transcription factor gene.

In certain embodiments, the ablation is effected by inserting the CAR into a locus of the cytokine/chemokine/transcription factor gene.

In certain embodiments, the CAR is part of a construct that also includes a selectable marker.

In certain embodiments, the cytokine deficiency is effected by deletion or suppression of the cytokine/chemokine/transcription factor gene, by Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), or Clustered Regularly Interspaces Short Palindromic Repeats (CRISPR) editing.

In certain embodiments, the cytokine deficiency is effected by suppression of the cytokine/chemokine/transcription factor gene transcript by transfection of small interfering RNAs (siRNAs).

Also disclosed herein is a chimeric antigen receptor (CAR)-bearing immune effector cell expressing at least one CAR, wherein:

-   -   the at least one CAR is inserted into a locus of a         cytokine/chemokine/transcription factor gene;     -   the cytokine/chemokine/transcription factor gene is deleted or         suppressed by a method chosen from Transcription Activator-like         Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), and         Clustered Regularly Interspaces Short Palindromic Repeats         (CRISPR) editing;     -   the cytokine is suppressed by expression of an scFv with an         endoplasmic reticulum (ER) binding tether to bind the cytokine         in the ER and prevent secretion; or     -   the cytokine/chemokine/transcription factor gene transcript is         suppressed by small interfering RNAs (siRNAs) transfection.

In certain embodiments, the cell is chosen from a chimeric antigen receptor T cell (CAR-T), a CAR-bearing iNKT cell (iNKT-CAR), and a CAR-bearing natural killer (NK) cell (NK-CAR).

In certain embodiments, the cell is a CAR-T.

In certain embodiments, the cell is a dual or tandem CAR-T.

In certain embodiments, the cell is an iNKT-CAR.

In certain embodiments, the cell is a dual or tandem iNKT-CAR.

In certain embodiments, the cytokine contributes to the development of cytokine release syndrome.

In certain embodiments, the cytokine is chosen from MCP1 (CCL2), MCP-2, GM-CSF, G-CSF, M-CSF, IL-4, and IFNγ.

In certain embodiments, the cytokine is GM-CSF.

In certain embodiments, the cell is a GM-CSF deficient CAR-T cell.

In certain embodiments, the cell is a GM-CSF deficient iNKT-CAR cell.

In certain embodiments, the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant T cell.

In certain embodiments, the antigen is selected from CD2, CD38, CD4, CD5, CD7, TCRA, and TCRβ.

In certain embodiments, the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant B cell.

In certain embodiments, the antigen is selected from CD19 and CD20.

In certain embodiments, the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant mesothelial cell.

In certain embodiments, the antigen is mesothelin.

In certain embodiments, the chimeric antigen receptor specifically binds at least one antigen expressed on a malignant plasma cell.

In certain embodiments, the antigen is selected from BCMA, CS1, CD38, and CD19.

In certain embodiments, the chimeric antigen receptor expresses the extracellular portion of the APRIL protein, the ligand for BCMA and TACI, effectively co-targeting both BCMA and TACI.

In certain embodiments, the CAR-T cell further comprises a suicide gene.

In certain embodiments, endogenous T cell receptor mediated signaling is negligible in the cell.

In certain embodiments, the cell does not induce alloreactivity or graft-versus-host disease.

In certain embodiments, the cell does not induce fratricide.

Also disclosed herein is a method of treatment of cancer in a patient, which has a reduced incidence of cytokine release syndrome and/or CAR-T associated neuropathy, comprising the administration of chimeric antigen receptor (CAR)-bearing immune effector cells as disclosed herein.

In certain embodiments, the cancer is a hematologic malignancy.

In certain embodiments, the hematologic malignancy is a T-cell malignancy.

In certain embodiments, the T cell malignancy is T-cell acute lymphoblastic leukemia (T-ALL).

In certain embodiments, the T cell malignancy is non-Hodgkin's lymphoma.

In certain embodiments, the hematologic malignancy is multiple myeloma.

In certain embodiments, the cancer is a solid tumor.

In certain embodiments, the cancer is cervical cancer, pancreatic cancer, ovarian cancer, mesothelioma, and lung cancer.

Also disclosed herein is a method of prevention or reduction of cytokine release syndrome, CAR-T associated neuropathy in a patient receiving chimeric antigen receptor T cell (CAR-T), CAR-bearing iNKT cell (iNKT-CAR), or CAR-bearing natural killer (NK) cell (NK-CAR) immunotherapy, comprising the administration of chimeric antigen receptor (CAR)-bearing immune effector cells as disclosed herein as the immunotherapy.

Also disclosed herein is a method of blocking the expression of a cytokine/chemokine/transcription factor gene in a chimeric antigen receptor T cell (CAR-T), CAR-bearing iNKT cell (iNKT-CAR), or CAR-bearing natural killer (NK) cell (NK-CAR), comprising the insertion of a CAR into a locus of the cytokine/chemokine/transcription factor gene.

CAR-Bearing Immune Effector Cells

A chimeric antigen receptor (CAR), is a recombinant fusion protein comprising: 1) an extracellular ligand-binding domain, i.e., an antigen-recognition domain, 2) a transmembrane domain, and 3) a signaling transducing domain.

Methods for CAR design, delivery and expression, and the manufacturing of clinical-grade CAR-T cell populations are known in the art. See, for example, Lee et al., Clin. Cancer Res., 2012, 18(10): 2780-90. An engineered chimeric antigen receptor polynucleotide that encodes for a CAR comprises: a signal peptide, an antigen recognition domain, at least one co-stimulatory domain, and a signaling domain.

The antigen-specific extracellular domain of a chimeric antigen receptor recognizes and specifically binds an antigen, typically a surface-expressed antigen of a malignancy. An “antigen-specific extracellular domain” (or, equivalently, “antigen-binding domain”) specifically binds an antigen when, for example, it binds the antigen with an affinity constant or affinity of interaction (KD) between about 0.1 pM to about 10 μM, preferably about 0.1 pM to about 1 μM, more preferably about 0.1 pM to about 100 nM. Methods for determining the affinity of interaction are known in the art. An antigen-specific extracellular domain suitable for use in a CAR of the present disclosure may be any antigen-binding polypeptide, a wide variety of which are known in the art. In some instances, the antigen-binding domain is a single chain Fv (scFv). Other antibody based recognition domains (cAb VHH (camelid antibody variable domains) and humanized versions thereof, lgNAR VH (shark antibody variable domains) and humanized versions thereof, sdAb VH (single domain antibody variable domains) and “camelized” antibody variable domains are suitable for use. In some instances, T-cell receptor (TCR) based recognition domains such as single chain TCR (scTv, single chain two-domain TCR containing VaVR) are also suitable for use.

A chimeric antigen receptor of the present disclosure also comprises an “intracellular domain” that provides an intracellular signal to the CAR-bearing immune effector cell upon antigen binding to the antigen-specific extracellular domain. The intracellular signaling domain of a chimeric antigen receptor of the present disclosure is responsible for activation of at least one of the effector functions of the T cell in which the chimeric receptor is expressed. The term “effector function” refers to a specialized function of a differentiated cell, such as an iNKT cell. An effector function of an iNKT cell, for example, may be NK transactivation, T cell activation and differentiation, B cell activation, dendritic cell activation and cross-presentation activity, and macrophage activation. Thus, the term “intracellular domain” refers to the portion of a CAR that transduces the effector function signal upon binding of an antigen to the extracellular domain and directs the iNKT cell to perform a specialized function. Non-limiting examples of suitable intracellular domains include the zeta chain of the T-cell receptor or any of its homologs (e.g., eta, delta, gamma, or epsilon), MB 1 chain, 829, Fe Rill, Fe R1, and combinations of signaling molecules, such as CD3ζ and CD28, CD27, 4-1 BB, DAP-10, OX40, and combinations thereof, as well as other similar molecules and fragments. Intracellular signaling portions of other members of the families of activating proteins may be used, such as FcγRIII and FcεRI. While usually the entire intracellular domain will be employed, in many cases it will not be necessary to use the entire intracellular polypeptide. To the extent that a truncated portion of the intracellular signaling domain may find use, such truncated portion may be used in place of the intact chain as long as it still transduces the effector function signal. The term intracellular domain is thus meant to include any truncated portion of the intracellular domain sufficient to transduce the effector function signal.

Typically, the antigen-specific extracellular domain is linked to the intracellular domain of the chimeric antigen receptor by a “transmembrane domain.” A transmembrane domain traverses the cell membrane, anchors the CAR to the T cell surface, and connects the extracellular domain to the intracellular signaling domain, thus impacting expression of the CAR on the T cell surface. Chimeric antigen receptors may also further comprise one or more costimulatory domain and/or one or more spacer. A “costimulatory domain” is derived from the intracellular signaling domains of costimulatory proteins that enhance cytokine production, proliferation, cytotoxicity, and/or persistence in vivo. A “peptide hinge” connects the antigen-specific extracellular domain to the transmembrane domain. The transmembrane domain is fused to the costimulatory domain, optionally a costimulatory domain is fused to a second costimulatory domain, and the costimulatory domain is fused to a signaling domain, not limited to CD3ζ. For example, inclusion of a spacer domain between the antigen-specific extracellular domain and the transmembrane domain, and between multiple scFvs in the case of tandem CAR, may affect flexibility of the antigen-binding domain(s) and thereby CAR function. Suitable transmembrane domains, costimulatory domains, and spacers are known in the art.

Engineered CARs may be introduced into CAR-bearing immune effector cells using retroviruses, which efficiently and stably integrate a nucleic acid sequence encoding the chimeric antigen receptor into the target cell genome. Other methods known in the art include, but are not limited to, lentiviral transduction, transposon-based systems, direct RNA transfection, and CRISPR/Cas systems (e.g., type I, type II, or type Ill systems using a suitable Cas protein such Cas3, Cas4, Cas5, Cas5e (or CasD), Cas6, Cas6e, Cas6f, Cas7, Cas8a1, Cas8a2, Cas8b, Cas8c, Cas9, Cas10, Cas1 Od, CasF, CasG, CasH, Csy1, Csy2, Csy3, Cse1 (or CasA), Cse2 (or CasB), Cse3 (or CasE), Cse4 (or CasC), Csc1, Csc2, Csa5, Csn2, Csm2, Csm3, Csm4, Csm5, Csm6, Cmr1, Cmr3, Cmr4, Cmr5, Cmr6, Csb1, Csb2, Csb3, Csx17, Csx14, Csx10, Csx16, CsaX, Csx3, Csz1, Csx15, Csf1, Csf2, Csf3, Csf4, and Cu1966, etc.). Zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) may also be used. See, e.g., Shearer R F and Saunders D N, “Experimental design for stable genetic manipulation in mammalian cell lines: lentivirus and alternatives,” Genes Cells 2015 January; 20(1):1-10.

Manipulation of PI3K signaling can be used to prevent altered CAR-T cell differentiation due to constitutive CAR self-signaling and foster long-lived memory T cell development. pharmacologic blockade of PI3K during CAR-T manufacture and ex vivo expansion can abrogate preferential effector T cell development and restore CAR-T effector/memory ratio to that observed in empty vector transduced T cells, which can improve in vivo T cell persistence and therapeutic activity. Inhibition of p110δ PI3K can enhance efficacy and memory in tumor-specific therapeutic CD8 T cells, while inhibition of p110α PI3K can increase cytokine production and antitumor response.

This is proposed to be because the presence of a CAR on a T cell's surface can alter its activation and differentiation, even in the absence of ligand. Constitutive self-signaling through CAR, related to both the scFv framework and the signaling domains, can lead to aberrant T cell behavior, including altered differentiation and decreased survival. This is significant as the effectiveness of CAR-T cells in patients is directly associated with their in vivo longevity. The presence of the CD28 costimulatory domain increased CAR-T cell exhaustion induced by persistent CAR self-signaling; the 4-1BB costimulatory domain had a lesser effect. Furthermore, CD3-zeta significantly enhances the constitutive activation of the PI3K, AKT, mTOR, and glycolysis pathways, and fostered formation of short-lived effector cells over central/stem memory cells. See, e.g., Zhang W. et al., “Modulation of PI3K signaling to improve CAR T cell function,” Oncotarget, 2018 Nov. 9; 9(88): 35807-35808.

CAR Antigens. Suitable antigens to be genome-edited in the iNKT cells disclosed herein, and to be recognized by the CARs of iNKT-CARs disclosed herein, include antigens specific to hematologic malignancies. These can include T cell-specific antigens and/or antigens that are not specific to T cells. The antigen may be specifically bound by the chimeric antigen receptor of an iNKT-CARs cell, and the antigen for which the iNKT-CARs cell is deficient, is an antigen expressed on a malignant T cell, preferably an antigen that is overexpressed on malignant T cell (i.e., a T cell derived from a T-cell malignancy) in comparison to a nonmalignant T cell. Examples of such antigens include CD2, CD3ε, CD4, CD5, CD7, TRAC, and TCRβ.

T-cell malignancies comprise malignancies derived from T-cell precursors, mature T cells, or natural killer cells. Examples of T-cell malignancies include T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), T-cell large granular lymphocyte (LGL) leukemia, human T-cell leukemia virus type 1-positive (HTLV-1+) adult T-cell leukemia/lymphoma (ATL), T-cell prolymphocytic leukemia (T-PLL), and various peripheral T-cell lymphomas (PTCLs), including but not limited to angioimmunoblastic T-cell lymphoma (AITL), ALK-positive anaplastic large cell lymphoma, and ALK-negative anaplastic large cell lymphoma.

Suitable CAR antigens can also include antigens found on the surface of a multiple myeloma cell, i.e., a malignant plasma cell, such as BCMA, CS1, CD38, and CD19. Alternatively, the CAR may be designed to express the extracellular portion of the APRIL protein, the ligand for BCMA and TACI, effectively co-targeting both BCMA and TACI for the treatment of multiple myeloma.

Additional examples of suitable antigens to be genome-edited in the iNKT cells disclosed herein, and to be recognized by the CARs of iNKT-CARs disclosed herein, are given below in Tables 1-10. These include CD2, CD3ε, CD4, CD5, CD7, TRAC, TCRβ, BCMA, CS1, and CD38.

Fratricide Resistance. The CAR-T, iNKT, NK and other CAR-bearing immune effector cells encompassed by the present disclosure are optionally deficient in one or more antigens to which the chimeric antigen receptor specifically binds and are therefore fratricide-resistant. In some embodiments, the one or more antigens of the cell is modified such the chimeric antigen receptor no longer specifically binds the one or more modified antigens. For example, the epitope of the one or more antigens recognized by the chimeric antigen receptor may be modified by one or more amino acid changes (e.g., substitutions or deletions) or the epitope may be deleted from the antigen. In other embodiments, expression of the one or more antigens is reduced in the cell by at least 50%, at least 60%, at least 70%, at least 80%, at least 90% or more. Methods for decreasing the expression of a protein are known in the art and include, but are not limited to, modifying or replacing the promoter operably linked to the nucleic acid sequence encoding the protein. In still other embodiments, the cell is modified such that the one or more antigens is not expressed, e.g., by deletion or disruption of the gene encoding the one or more antigens. In each of the above embodiments, the CAR-bearing immune effector cell may be deficient in one or preferably all the antigens to which the chimeric antigen receptor specifically binds. Methods for genetically modifying a cell to be deficient in one or more antigens are well known in art, and non-limiting examples are provided above. In an exemplary embodiment, CRISPR/cas9 gene editing can be used to modify a cell to be deficient in one or more antigens. Zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) may also be used. See, e.g., Shearer RF and Saunders D N, “Experimental design for stable genetic manipulation in mammalian cell lines: lentivirus and alternatives,” Genes Cells 2015 January; 20(1):1-10.

Avoidance of Allogenicity. CAR-T, iNKT, NK and other CAR-bearing immune effector cells encompassed by the present disclosure may further be deficient in endogenous T cell receptor (TCR) signaling as a result of deleting a part of the T Cell Receptor (TCR)-CD3 complex. In various embodiments it may be desirable to eliminate or suppress endogenous TCR signaling in CAR-bearing immune effector cells disclosed herein. For example, decreasing or eliminating endogenous TCR signaling in CAR-T cells may prevent or reduce graft versus host disease (GvHD) when allogenic T cells are used to produce the CAR-T cells. Methods for eliminating or suppressing endogenous TCR signaling are known in the art and include, but are not limited to, deleting a part of the TCR-CD3 receptor complex, e.g., the TCR receptor alpha chain (TRAC), the TCR receptor beta chain (TRBC), CD3ε CD3γ CD3δ, and/or CD3ζ. Deleting a part of the TCR receptor complex may block TCR mediated signaling and may thus permit the safe use of allogeneic T cells as the source of CAR-T cells without inducing life-threatening GvHD.

Suicide Genes. Alternatively, or in addition, CAR-bearing immune effector cells encompassed by the present disclosure may further comprise one or more suicide genes. As used herein, “suicide gene” refers to a nucleic acid sequence introduced to a cell by standard methods known in the art that, when activated, results in the death of the cell. Suicide genes may facilitate effective tracking and elimination of the CAR-bearing immune effector cells in vivo if required. Facilitated killing by activating the suicide gene may occur by methods known in the art. Suitable suicide gene therapy systems known in the art include, but are not limited to, various the herpes simplex virus thymidine kinase (HSVtk)/ganciclovir (GCV) suicide gene therapy systems or inducible caspase 9 protein. In an exemplary embodiment, a suicide gene is a CD34/thymidine kinase chimeric suicide gene.

Components that may be included in a CAR as described herein are provided below in Tables 1 and 2.

TABLE 1 Amino acid sequences of different CAR components. SEQ ID Functional domains NO:  Amino acid sequence CD8α signal peptide SEQ ID MALPVTALLLPLALLLHAARP NO: 1 CD8α hinge SEQ ID TTTPAPRPPTPAPTIASQPLSLRPEACR NO: 2 VPAAGGAHTRGLDFACD CD28 Transmembrane SEQ ID FWVLVVVGGVLACYSLLVTVAFIIFWV (Tm) domain NO: 3 Surface SEQ ID MALPVTALLLPLALLLHAARPSQFRVSPLDRT glycoprotein CD8 NO: 4 WNLGETVELKCQVLLSNPTSGCSWLFQPRGAA alpha chain ASPTFLLYLSQNKPKAAEGLDTQRFSGKRLGDT isoform 1 FVLTLSDFRRENEGYYFCSALSNSIMYFSHFVP precursor VFLPAKPTTTPAPRPPTPAPTIASQPLSLRPEACR (NP_001139345.1) PAAGGAVHTRGLDFACDIYIWAPLAGTCGVLL LSLVITLYCNHRNRRRVCKCPRPVVKSGDKPSL SARYV 4-1BB costimulatory SEQ ID KRGRKKLLYIFKQPFMRPVQTTQEEDGCSCRFP domain NO: 5 EEEEGGCEL CD28 costimulatory SEQ ID RSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAP domain NO: 6 PRDFAAYRS CD3 zeta (ζ) SEQ ID RVKFSRSADAPAYKQGQNQLYNELNLGRREEY NO: 7 DVLDKRRGRDPEMGGKPRRKNPQEGLYNELQ KDKMAEAYSEIGMKGERRRGKGHDGLYQGLS TATKDTYDALHMQALPPR P2A peptide SEQ ID GSGATNFSLLKQAGDVEENPGP NO: 8 (GGGGS)₄ linker SEQ ID GGGGSGGGGSGGGGSGGGGS NO: 9 hCD34 SEQ ID MPRGWTALCLLSLLPSGFMSLDNNGTATPELP NO: 10 TQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQ HGNEATTNITETTVKFTSTSVITSVYGNTNSSVQ SQTSVISTVFTTPANVSTPETTLKPSLSPGNVSD LSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSG IREVKLTQGICLEQNKTSSCAEFKKDRGEGLARV LCGEEQADADAGAQVCSLLLAQSEVRPQCLLL VLANRTEISSKLQLMKKHQSDLKKLGILDFTEQ DVASHQSYSQKTLIALVTSGALLAVLGITGYFL MNRRSWSPI Human-Herpes Simplex SEQ ID MPRGWTALCLLSLLPSGFMSLDNNGTATPELP Virus-1 (HSV)- NO: 11 TQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQ thymidine HGNEATTNITETTVKFTSTSVITSVYGNTNSSVQ kinase (TK) SQTSVISTVFTTPANVSTPETTLKPSLSPGNVSD LSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSG IREVKLTQGICLEQNKTSSCAEFKKDRGEGLARV LCGEEQADADAGAQVCSLLLAQSEVRPQCLLL VLANRTEISSKLQLMKKHQSDLKKLGILDFTEQ DVASHQSYSQKTLIALVTSGALLAVLGITGYFL MNRRSWSPTGEGGGGGDLGGVKLPHLFGKRL VEARMASYPCHQHASAFDQAARSRGHSNRRT ALRPRRQQEATEVRLEQKMPTLLRVYIDGPHG MGKTTTTQLLVALGSRDDIVYVPEPMTYWQV LGASETIANIYTTQHRLDQGEISAGDAAVVMTS AQITMGMPYAVTDAVLAPHVGGEAGSSHAPPP ALTLLLDRHPIAVMLCYPAARYLMGSMTPQAV LAFVALIPPTLPGTNIVLGALPEDRHIDRLAKRQ RPGERLDLAMLAAIRRVYGLLANTVRYLQGGG SWWEDWGQLSGTAVPPQGAEPQSNAGPRPHIG DTLFTLFRAPELLAPNGDLYNVFAWALDVLAK RLRPMHVFILDYDQSPAGCRDALLQLTSGMVQ THVTTPGSIPTICDLARTFAREMGEAN

TABLE 2 Amino acid sequences of the variable heavy (V_(H)) and variable light (V_(L)) chains of the scFvs. SEQ ID ScFv sequences NO:  Amino acid sequence CD2 heavy chain variable SEQ ID EVKLEESGAELVKPGASVKLSCRTSGFNIKDTI region (35.1 ATCC®HB- NO: 12 HWVKQRPEQGLKWIGRIDPANGNTKYDPKFQ 222™) DKATVTADTSSNTAYLQLSSLTSEDTAVYYCV TYAYDGNWYFDVWGAGTAVTVSS CD2 light chain variable SEQ ID DIKNITQSPSSMYVSLGERVTITCKASQDINSFL region (35.1 ATCC®HB- NO: 13 SWFQQKPGKSPKTLIYRANRLVDGVPSRFSGS 222™) GSGQDYSLTISSLEYEDMEIYYCLQYDEFPYTF GGGTKLEMKR CD2 heavy chain variable SEQ ID EVQLEESGAELVRPGTSVKLSCKASGYTFTSY region (OKT 11 NO: 14 WMHWIKQRPEQGLEWIGRIDPYDSETHYNEK ATCC®CRL-8027™) FKDKAILSVDKSSSTAYIQLSSLTSDDSAVYYC SRRDAKYDGYALDYWGQGTSVTVSS CD2 light chain variable SEQ ID DFVMTQAAPSVPVTPGESVSISCRSSKTLLHSN region (OKT 11 NO: 15 GNTYLYWFLQRPGQSPQVLIYRMSNLASGVP ATCC®CRL-8027™) NRFSGSGSETTFTLRISRVEAEDVGIYYCMQHL EYPYTFGGGTKLEIER CD3 heavy chain variable SEQ ID GSQVQLQQSGAELARPGASVKMSCKASGYTF region (OKT 3) NO: 16 TRYTMHWVKQRPGQGLEWIGYINPSRGYTNY NQKFKDKATLTTDKSSSTAYMQLSSLTSEDSA VYYCARYYDDHYCLDYWGQGTTLTVSS CD3 light chain variable SEQ ID QFVLTQSPAIMSASPGEKVTMTCSASSSVSYM region (OKT 3) NO: 17 NWYQQKSGTSPKRWIYDTSKLASGVPAHFRG SGSGTSYSLTISGMEAEDAATYYCQQWSSNPF TFGSGTKLEINR CD3 heavy chain variable SEQ ID EVQLVESGGGLVQPGGSLRLSCAASGYSFTGY region (UCHT1) NO: 18 TMNWVRQAPGKCLEWVALINPYKGVSTYNQ KFKDRFTISVDKSKNTAYLQMNSLRAEDTAV YYCARSGYYGDSDWYFDVWGQGTLVTVSS CD3 heavy chain variable SEQ ID DIQMTQSPSSLSASVGDRVTITCRASQDIRNYL region (UCHT1) NO: 19 NWYQQKPGKAPKLLIYYTSRLESGVPSRFSGS GSGTDYTLTISSLQPEDFATYYCQQGNTLPWT FGCGTKVEIK CD7 heavy chain variable SEQ ID EVQLVESGGGLVKPGGSLKLSCAASGLTFSSY region NO: 20 AMSWVRQTPEKRLEWVASISSGGFTYYPDSV KGRFTISRDNARNILYLQMSSLRSEDTAMYYC ARDEVRGYLDVWGAGTTVTVS CD7 light chain variable SEQ ID DIQMTQTTSSLSASLGDRVTISCSASQGISNYL region NO: 21 NWYQQKPDGTVKLLIYYTSSLHSGVPSRFSGS GSGTDYSLTISNLEPEDIATYYCQQYSKLPYTF GGGTKLEIKR FTL3 heavy chain SEQ ID EVQLVQSGAEVKKPGASVKVSCKASGYTFTS variable region (EB10) NO: 22 YYMHWVRQAPGQGLEWMGIINPSGGSTSYAQ KFQGRVTMTRDTSTSTVYMELSSLRSEDTAVY YCARGVGAHDAFDIWGQGTTVTVSS FTL3 light chain variable SEQ ID DVVMTQSPLSLPVTPGEPASISCRSSQSLLHSN region (EB10) NO: 23 GNNYLDWYLQKPGQSPQLLIYLGSNRASGVP DRFSGSGSDTDFTLQISRVEAEDVGVYYCMQG THPAISFGQGTRLEIK FTL3 heavy chain SEQ ID EVQLVQSGAEVKKPGSSVKVSCKASGGTFSSY variable region (NC7) NO: 24 AISWVRQAPGQGLEWMGGIIPIFGTANYAQKF QGRVTITADKSTSTAYMELSSLRSEDTAVYYC ATFALFGFREQAFDIWGQGTTVTVSS FTL3 light chain variable SEQ ID DIQMTQSPSSLSASVGDRVTITCRASQSISSYLN region (NC7) NO: 25 WYQQKPGKAPKLLIYAASSLQSGVPSRFSGSG SGTDFTLTISSLQPEDLATYYCQQSYSTPFTFGP GTKVDIK FTL3 heavy chain SEQ ID EVQLVQSGAEVKKPGASVKVSCKASGYTFTS variable region (D3-D4) NO: 26 YYMHWARQAPGQGLEWMGIINPSGGSTSYAQ KFQGRVTMTRDTSTSTVYMELSSLRSEDTAVY YCARVVAAAVADYWGQGTLVTVS S FTL3 light chain variable SEQ ID DVVMTQSPLSLPVTPGEPASISCRSSQSLLHSN region (D3-D4) NO: 27 GYNYLDWYLQKPGQSPQLLIYLGSNRASGVP DRFSGSGSGTDFTLKISRVEAEDVGVYYCMQS LQTPFTFGPGTKVDIK CS1 heavy chain variable SEQ ID QVQLQQPGAELVRPGASVKLSCKASGYSFTTY region NO: 28 WMNWVKQRPGQGLEWIGMIHPSDSETRL NQKFKDKATLTVDKSSSTAYMQLSSPTSEDSA VYYCARSTMIATRAMDYWGQGTSVTVSS CS1 light chain variable SEQ ID DIVMTQSQKSMSTSVGDRVSITCKASQDVITG region NO: 29 VAWYQQKPGQSPKLLIYSASYRYTGVPD RFTGSGSGTDFTFTISNVQAEDLAVYYCQQHY STPLTFGAGTKLELK CD33 heavy chain SEQ ID QVQLQQPGAEVVKPGASVKMSCKASGYTFTS variable region NO: 30 YYIHWIKQTPGQGLEWVGVIYPGNDDISYNQK FQGKATLTADKSSTTAYMQLSSLTSEDSAVYY CAREVRLRYFDVWGQGTTVTVSSSG CD33 light chain variable SEQ ID GSEIVLTQSPGSLAVSPGERVTMSCKSSQSVFF region NO: 31 SSSQKNYLAWYQQIPGQSPRLLIYWASTRESG VPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQ YLSSRTFGQGTKLEIKR

Mono CAR-T Cells

In certain embodiments, the disclosure provides an engineered T cell comprising a single CAR, that specifically binds an antigen or cell surface protein, wherein the T cell is optionally deficient in that antigen or cell surface protein (e.g., CD7CARTΔCD7 cell). In non-limiting examples, the deficiency in the antigen or cell surface protein resulted from (a) modification of antigen or cell surface protein expressed by the T cell such that the chimeric antigen receptors no longer specifically binds the modified antigen or cell surface protein (e.g., the epitope of the one or more antigens recognized by the chimeric antigen receptor may be modified by one or more amino acid changes (e.g., substitutions or deletions) or the epitope may be deleted from the antigen), (b) modification of the T cell such that expression of antigen or cell surface protein is reduced in the T cell by at least 50%, at least 60%, at least 70%, at least 80%, at least 90% or more, or (c) modification of the T cell such that antigen or cell surface protein is not expressed (e.g., by deletion or disruption of the gene encoding antigen or cell surface protein). In each of the above embodiments, the CAR-T cell may be deficient in one or preferably all the antigens or cell surface proteins to which the chimeric antigen receptor specifically binds. The methods to genetically modify a T cell to be deficient in one or more antigens or cell surface proteins are well known in art and non-limiting examples are provided herein. In embodiments described below, the CRISPR-Cas9 system is used to modify a T cell to be deficient in one or more antigens. Any of these may be accomplished by the methods disclosed herein. In further embodiments, the T cell comprises a suicide gene.

For example, the CAR for a CD7 specific CAR-T cell may be generated by cloning a commercially synthesized anti-CD7 single chain variable fragment (scFv) into a 3rd generation CAR backbone with CD28 and/or 4-1BB internal signaling domains. An extracellular hCD34 domain may be added after a P2A peptide to enable both detection of CAR following viral transduction and purification using anti-hCD34 magnetic beads. A similar method may be followed for making CARs specific for other malignant T cell antigens.

CAR-T cells encompassed by the present disclosure may further be deficient in endogenous T cell receptor (TCR) signaling as a result of deleting a part of the T Cell Receptor (TCR)-CD3 complex. In various embodiments it may be desirable to eliminate or suppress endogenous TCR signaling in CAR-T cells disclosed herein. For example, decreasing or eliminating endogenous TCR signaling in CAR-T cells may prevent or reduce graft versus host disease (GvHD) when allogenic T cells are used to produce the CAR-T cells. Methods for eliminating or suppressing endogenous TCR signaling are known in the art and include, but are not limited to, deleting a part of the TCR-CD3 receptor complex, e.g., the TCR receptor alpha chain (TRAC), the TCR receptor beta chain (TCRβ) or subtypes thereof, TCRδ, TCRγ, CD3ε, CD3γ, and/or CD3δ. Deleting a part of the TCR receptor complex may block TCR mediated signaling and may thus permit the safe use of allogeneic T cells as the source of CAR-T cells without inducing life-threatening GvHD.

In addition, the CAR-T cells encompassed by the present disclosure may further comprise one or more suicide genes as described herein.

In a similar manner, other mono-CAR-T cells may be constructed and are given below in Table 3.

TABLE 3 Mono CARs and CAR-Ts Antigen Target Antigen Deletion/ Example of CAR-T cells Suppression M1 APRIL — M2 APRIL APRIL M3 APRIL APRIL + TRAC M4 APRIL APRIL + CD3ε M5 APRIL CD3ε M6 BCMA — M7 CD117 — M8 CD117 CD117 M9 CD123 — M10 CD123 CD123 M11 CD135 — M12 CD135 CD135 M13 CD138 — M14 CD19 — M15 CD1a — M16 CD1a CD3ε M17 CD1a TRAC M18 CD1a CD1a + TRAC M19 CD1a CD1a + CD3ε M20 CD2 — M21 CD2 CD2 M22 CD2 CD2 + TRAC M23 CD2 CD2 + CD3ε M24 CD20 M25 CD21 M26 CD22 M27 CD23 M28 CD3 — M29 CD3 CD3ε M30 CD3 CD3ε + TRAC M31 CD33 — M32 CD33 CD33 M33 CD371 — M34 CD371 CD371 M35 CD38 — M36 CD38 CD38 M37 CD4 — M38 CD4 CD4 M39 CD4 CD4 + TRAC M40 CD4 CD4 + CD3ε M41 CD5 — M42 CD5 CD5 M43 CD5 CD5 + TRAC M44 CD5 CD5 + CD3ε M45 CD56 — M46 CD56 CD56 M47 CD56 CD56 + TRAC M48 CD56 CD56 + CD3ε M49 CD56 CD3ε M50 CD56 TRAC M51 CD7 — M52 CD7 CD7 M53 CD7 CD7 + TRAC M54 CD7 CD7 + CD3ε M55 CD79A — M56 CD79B — M57 CS1 — M58 CS1 CS1 M59 Tim-3 — M60 Tim-3 Tim-3 M61 Tim-3 Tim-3 + TRAC M62 Tim-3 TRAC M63 Tim-3 CD3ε M64 Tim-3 Tim-3 + CD3ε

Disclosed are embodiments of CAR amino acid sequences that can be expressed on the surface of a genome-edited CAR-T cell derived from a cytotoxic T cell, a memory T cell, or a gamma delta (γδ) T cell.

TABLE 4 Amino Acid Sequences of Mono Chimeric Antigen Receptors (CARs). Mono CAR SEQ ID Constructs NO:  Amino acid sequence CD7-CAR-4- SEQ ID MALPVTALLLPLALLLHAARPDIQMTQTTSSLSASLGDRVT 1BB_CD34 NO: 32 ISCSASQGISNYLNWYQQKPDGTVKLLIYYTSSLHSGVPSRF SGSGSGTDYSLTISNLEPEDIATYYCQQYSKLPYTFGGGTKL EIKRGGGGSGGGGSGGGGSGGGGSEVQLVESGGGLVKPG GSLKLSCAASGLTFSSYAMSWVRQTPEKRLEWVASISSGGF TYYPDSVKGRFTISRDNARNILYLQMSSLRSEDTAMYYCA RDEVRGYLDVWGAGTTVTVSPRASTTTPAPRPPTPAPTIAS QPLSLRPEACRPAAGGAVHTRGLDFACDFWVLVVVGGVL ACYSLLVTVAFIIFWVKRGRKKLLYIFKQPFMRPVQTTQEE DGCSCRFPEEEEGGCELRVKFSRSADAPAYKQGQNQLYNE LNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNEL QKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTY DALHMQALPPRRTDGSGATNFSLLKQAGDVEENPGPVSEA MPRGWTALCLLSLLPSGFMSLDNNGTATPELPTQGTFSNVS TNVSYQETTTPSTLGSTSLHPVSQHGNEATTNITETTVKFTS TSVITSVYGNTNSSVQSQTSVISTVFTTPANVSTPETTLKPSL SPGNVSDLSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSGI REVKLTQGICLEQNKTSSCAEFKKDRGEGLARVLCGEEQADA DAGAQVCSLLLAQSEVRPQCLLLVLANRTEISSKLQLMKK HQSDLKKLGILDFTEQDVASHQSYSQKTLIALVTSGALLAV LGITGYFLMNRRSWSPI CD7-CAR-4- SEQ ID MALPVTALLLPLALLLHAARPDIQMTQTTSSLSASLGDRVT 1BB_CD34_TK NO: 33 ISCSASQGISNYLNWYQQKPDGTVKLLIYYTSSLHSGVPSRF SGSGSGTDYSLTISNLEPEDIATYYCQQYSKLPYTFGGGTKL EIKRGGGGSGGGGSGGGGSGGGGSEVQLVESGGGLVKPG GSLKLSCAASGLTFSSYAMSWVRQTPEKRLEWVASISSGGF TYYPDSVKGRFTISRDNARNILYLQMSSLRSEDTAMYYCA RDEVRGYLDVWGAGTTVTVSPRASTTTPAPRPPTPAPTIAS QPLSLRPEACRPAAGGAVHTRGLDFACDFWVLVVVGGVL ACYSLLVTVAFIIFWVKRGRKKLLYIFKQPFMRPVQTTQEE DGCSCRFPEEEEGGCELRVKFSRSADAPAYKQGQNQLYNE LNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNEL QKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTY DALHMQALPPRRTDGSGATNFSLLKQAGDVEENPGPVSEA MPRGWTALCLLSLLPSGFMSLDNNGTATPELPTQGTFSNVS TNVSYQETTTPSTLGSTSLHPVSQHGNEATTNITETTVKFTS TSVITSVYGNTNSSVQSQTSVISTVFTTPANVSTPETTLKPSL SPGNVSDLSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSGIRE VKLTQGICLEQNKTSSCAEFKKDRGEGLARVLCGEEQADA DAGAQVCSLLLAQSEVRPQCLLLVLANRTEISSKLQLMKK HQSDLKKLGILDFTEQDVASHQSYSQKTLIALVTSGALLAV LGITGYFLMNRRSWSPTGEGGGGGDLGGVKLPHLFGKRLV EARMASYPCHQHASAFDQAARSRGHSNRRTALRPRRQQE ATEVRLEQKMPTLLRVYIDGPHGMGKTTTTQLLVALGSRD DIVYVPEPMTYWQVLGASETIANIYTTQHRLDQGEISAGDA AVVMTSAQITMGMPYAVTDAVLAPHVGGEAGSSHAPPPA LTLLLDRHPIAVMLCYPAARYLMGSMTPQAVLAFVALIPPT LPGTNIVLGALPEDRHIDRLAKRQRPGERLDLAMLAAIRRV YGLLANTVRYLQGGGSWWEDWGQLSGTAVPPQGAEPQS NAGPRPHIGDTLFTLFRAPELLAPNGDLYNVFAWALDVLA KRLRPMHVFILDYDQSPAGCRDALLQLTSGMVQTHVTTPG SIPTICDLARTFAREMGEAN CD7-CAR- SEQ ID MALPVTALLLPLALLLHAARPDIQMTQTTSSLSASLGDRVT CD28_CD34 NO: 34 ISCSASQGISNYLNWYQQKPDGTVKLLIYYTSSLHSGVPSRF SGSGSGTDYSLTISNLEPEDIATYYCQQYSKLPYTFGGGTKL EIKRGGGGSGGGGSGGGGSGGGGSEVQLVESGGGLVKPG GSLKLSCAASGLTFSSYAMSWVRQTPEKRLEWVASISSGGF TYYPDSVKGRFTISRDNARNILYLQMSSLRSEDTAMYYCA RDEVRGYLDVWGAGTTVTVSPRASTTTPAPRPPTPAPTIAS QPLSLRPEACRPAAGGAVHTRGLDFACDFWVLVVVGGVL ACYSLLVTVAFIIFWVRSKRSRLLHSDYMNMTPRRPGPTRK HYQPYAPPRDFAAYRSRVKFSRSADAPAYKQGQNQLYNE LNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNEL QKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTY DALHMQALPPRRTDGSGATNFSLLKQAGDVEENPGPVSEA MPRGWTALCLLSLLPSGFMSLDNNGTATPELPTQGTFSNVS TNVSYQETTTPSTLGSTSLHPVSQHGNEATTNITETTVKFTS TSVITSVYGNTNSSVQSQTSVISTVFTTPANVSTPETTLKPSL SPGNVSDLSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSGIRE VKLTQGICLEQNKTSSCAEFKKDRGEGLARVLCGEEQADA DAGAQVCSLLLAQSEVRPQCLLLVLANRTEISSKLQLMKK HQSDLKKLGILDFTEQDVASHQSYSQKTLIALVTSGALLAV LGITGYFLMNRRSWSPI CD7-CAR- SEQ ID MALPVTALLLPLALLLHAARPDIQMTQTTSSLSASLGDRVT CD28_CD34_TK NO: 35 ISCSASQGISNYLNWYQQKPDGTVKLLIYYTSSLHSGVPSRF SGSGSGTDYSLTISNLEPEDIATYYCQQYSKLPYTFGGGTKL EIKRGGGGSGGGGSGGGGSGGGGSEVQLVESGGGLVKPG GSLKLSCAASGLTFSSYAMSWVRQTPEKRLEWVASISSGGF TYYPDSVKGRFTISRDNARNILYLQMSSLRSEDTAMYYCA RDEVRGYLDVWGAGTTVTVSPRASTTTPAPRPPTPAPTIAS QPLSLRPEACRPAAGGAVHTRGLDFACDFWVLVVVGGVL ACYSLLVTVAFIIFWVRSKRSRLLHSDYMNMTPRRPGPTRK HYQPYAPPRDFAAYRSRVKFSRSADAPAYKQGQNQLYNE LNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEGLYNEL QKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTY DALHMQALPPRRTDGSGATNFSLLKQAGDVEENPGPVSEA MPRGWTALCLLSLLPSGFMSLDNNGTATPELPTQGTFSNVS TNVSYQETTTPSTLGSTSLHPVSQHGNEATTNITETTVKFTS TSVITSVYGNTNSSVQSQTSVISTVFTTPANVSTPETTLKPSL SPGNVSDLSTTSTSLATSPTKPYTSSSPILSDIKAEIKCSGIRE VKLTQGICLEQNKTSSCAEFKKDRGEGLARVLCGEEQADA DAGAQVCSLLLAQSEVRPQCLLLVLANRTEISSKLQLMKK HQSDLKKLGILDFTEQDVASHQSYSQKTLIALVTSGALLAV LGITGYFLMNRRSWSPTGEGGGGGDLGGVKLPHLFGKRLV EARMASYPCHQHASAFDQAARSRGHSNRRTALRPRRQQE ATEVRLEQKMPTLLRVYIDGPHGMGKTTTTQLLVALGSRD DIVYVPEPMTYWQVLGASETIANIYTTQHRLDQGEISAGDA AVVMTSAQITMGMPYAVTDAVLAPHVGGEAGSSHAPPPA LTLLLDRHPIAVMLCYPAARYLMGSMTPQAVLAFVALIPPT LPGTNIVLGALPEDRHIDRLAKRQRPGERLDLAMLAAIRRV YGLLANTVRYLQGGGSWWEDWGQLSGTAVPPQGAEPQS NAGPRPHIGDTLFTLFRAPELLAPNGDLYNVFAWALDVLA KRLRPMHVFILDYDQSPAGCRDALLQLTSGMVQTHVTTPG SIPTICDLARTFAREMGEAN CD79B-CAR- SEQ ID MALPVTALLLPLALLLHAARPGSDIQLTQSPSSLSASVGDR CD28_CD34 NO: 36 VTITCKASQSVDYEGDSFLNWYQQKPGKAPKLLIYAASNL ESGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSNEDPL TFGQGTKVEIKRGGGGSGGGGSGGGGSGGGGSGGGGSEV QLVESGGGLVQPGGSLRLSCAASGYTFSSYWIEWVRQAPG KGLEWIGEILPGGGDTNYNEIFKGRATFSADTSKNTAYLQM NSLRAEDTAVYYCTRRVPIRLDYWGQGTLVTVSSPRASTT TPAPRPPTPAPTIASQPLSLRPEACRPAAGGAVHTRGLDFAC DFWVLVVVGGVLACYSLLVTVAFIIFWVRSKRSRLLHSDY MNMTPRRPGPTRKHYQPYAPPRDFAAYRSRVKFSRSADAP AYKQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPR RKNPQEGLYNELQKDKMAEAYSEIGMKGERRRGKGHDGL YQGLSTATKDTYDALHMQALPPRRTDGSGATNFSLLKQAG DVEENPGPVSEAMPRGWTALCLLSLLPSGFMSLDNNGTAT PELPTQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQHGNEA TTNITETTVKFTSTSVITSVYGNTNSSVQSQTSVISTVFTTPA NVSTPETTLKPSLSPGNVSDLSTTSTSLATSPTKPYTSSSPILS DIKAEIKCSGIREVKLTQGICLEQNKTSSCAEFKKDRGEGLA RVLCGEEQADADAGAQVCSLLLAQSEVRPQCLLLVLANRT EISSKLQLMKKHQSDLKKLGILDFTEQDVASHQSYSQKTLI ALVTSGALLAVLGITGYFLMNRRSWSPTGEGGGGGFKRDL GGVKLPHLFGKRLVEARMASYPCHQHASAFDQAARSRGH SNRRTALRPRRQQEATEVRLEQKMPTLLRVYIDGPHGMGK TTTTQLLVALGSRDDIVYVPEPMTYWQVLGASETIANIYTT QHRLDQGEISAGDAAVVMTSAQITMGMPYAVTDAVLAPH VGGEAGSSHAPPPALTLLLDRHPIAVMLCYPAARYLMGSM TPQAVLAFVALIPPTLPGTNIVLGALPEDRHIDRLAKRQRPG ERLDLAMLAAIRRVYGLLANTVRYLQGGGSWWEDWGQL SGTAVPPQGAEPQSNAGPRPHIGDTLFTLFRAPELLAPNGD LYNVFAWALDVLAKRLRPMHVFILDYDQSPAGCRDALLQ LTSGMVQTHVTTPGSIPTICDLARTFAREMGEAN CD2-CAR- SEQ ID MALPVTALLLPLALLLHAARPDIVMTQAAPSVPVTPGESVS CD28_CD34 NO: 37 ISCRSSKTLLHSNGNTYLYWFLQRPGQSPQVLIYRMSNLAS GVPNRFSGSGSETTFTLRISRVEAEDVGIYYCMQHLEYPYT FGGGTKLEIERGGGGSGGGGSGGGGSGGGGSEVQLEESGA ELVRPGTSVKLSCKASGYTFTSYWMHWIKQRPEQGLEWIG RIDPYDSETHYNEKFKDKAILSVDKSSSTAYIQLSSLTSDDS AVYYCSRRDAKYDGYALDYWGQGTSVTVSSPRASTTTPA PRPPTPAPTIASQPLSLRPEACRPAAGGAVHTRGLDFACDF WVLVVVGGVLACYSLLVTVAFIIFWVRSKRSRLLHSDYMN MTPRRPGPTRKHYQPYAPPRDFAAYRSRVKFSRSADAPAY KQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRK NPQEGLYNELQKDKMAEAYSEIGMKGERRRGKGHDGLYQ GLSTATKDTYDALHMQALPPRRTDGSGATNFSLLKQAGDV EENPGPVSEAMPRGWTALCLLSLLPSGFMSLDNNGTATPEL PTQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQHGNEATT NITETTVKFTSTSVITSVYGNTNSSVQSQTSVISTVFTTPANV STPETTLKPSLSPGNVSDLSTTSTSLATSPTKPYTSSSPILSDI KAEIKCSGIREVKLTQGICLEQNKTSSCAEFKKDRGEGLAR VLCGEEQADADAGAQVCSLLLAQSEVRPQCLLLVLANRTE ISSKLQLMKKHQSDLKKLGILDFTEQDVASHQSYSQKTLIA LVTSGALLAVLGITGYFLMNRRSWSPI CD2-CAR-4- SEQ ID MALPVTALLLPLALLLHAARPDIVMTQAAPSVPVTPGESVS 1BB_CD34 NO: 38 ISCRSSKTLLHSNGNTYLYWFLQRPGQSPQVLIYRMSNLAS GVPNRFSGSGSETTFTLRISRVEAEDVGIYYCMQHLEYPYT FGGGTKLEIERGGGGSGGGGSGGGGSGGGGSEVQLEESGA ELVRPGTSVKLSCKASGYTFTSYWMHWIKQRPEQGLEWIG RIDPYDSETHYNEKFKDKAILSVDKSSSTAYIQLSSLTSDDS AVYYCSRRDAKYDGYALDYWGQGTSVTVSSPRASTTTPA PRPPTPAPTIASQPLSLRPEACRPAAGGAVHTRGLDFACDF WVLVVVGGVLACYSLLVTVAFIIFWVKRGRKKLLYIFKQP FMRPVQTTQEEDGCSCRFPEEEEGGCELRVKFSRSADAPAY KQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRK NPQEGLYNELQKDKMAEAYSEIGMKGERRRGKGHDGLYQ GLSTATKDTYDALHMQALPPRRTDGSGATNFSLLKQAGDV EENPGPVSEAMPRGWTALCLLSLLPSGFMSLDNNGTATPEL PTQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQHGNEATT NITETTVKFTSTSVITSVYGNTNSSVQSQTSVISTVFTTPANV STPETTLKPSLSPGNVSDLSTTSTSLATSPTKPYTSSSPILSDI KAEIKCSGIREVKLTQGICLEQNKTSSCAEFKKDRGEGLAR VLCGEEQADADAGAQVCSLLLAQSEVRPQCLLLVLANRTE ISSKLQLMKKHQSDLKKLGILDFTEQDVASHQSYSQKTLIA LVTSGALLAVLGITGYFLMNRRSWSPI CD3-CD28-CD34 SEQ ID MALPVTALLLPLALLLHAARPGSQVQLQQSGAELARPGAS NO: 39 VKMSCKASGYTFTRYTMHWVKQRPGQGLEWIGYINPSRG YTNYNQKFKDKATLTTDKSSSTAYMQLSSLTSEDSAVYYC ARYYDDHYCLDYWGQGTTLTVSSGGGGSGGGGSGGGGS GGGGSQIVLTQSPAIMSASPGEKVTMTCSASSSVSYMNWY QQKSGTSPKRWIYDTSKLASGVPAHFRGSGSGTSYSLTISG MEAEDAATYYCQQWSSNPFTFGSGTKLEINRPRASTTTPAP RPPTPAPTIASQPLSLRPEACRPAAGGAVHTRGLDFACDFW VLVVVGGVLACYSLLVTVAFIIFWVRSKRSRLLHSDYMNM TPRRPGPTRKHYQPYAPPRDFAAYRSRVKFSRSADAPAYK QGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRKN PQEGLYNELQKDKMAEAYSEIGMKGERRRGKGHDGLYQG LSTATKDTYDALHMQALPPRRTDGSGATNFSLLKQAGDVE ENPGPVSEAMPRGWTALCLLSLLPSGFMSLDNNGTATPELP TQGTFSNVSTNVSYQETTTPSTLGSTSLHPVSQHGNEATTNI TETTVKFTSTSVITSVYGNTNSSVQSQTSVISTVFTTPANVST PETTLKPSLSPGNVSDLSTTSTSLATSPTKPYTSSSPILSDI KAEIKCSGIREVKLTQGICLEQNKTSSCAEFKKDRGEGLARVL CGEEQADADAGAQVCSLLLAQSEVRPQCLLLVLANRTEISS KLQLMKKHQSDLKKLGILDFTEQDVASHQSYSQKTLIALV TSGALLAVLGITGYFLMNRRSWSPI

Tandem CAR-T Cells

A tandem CAR-T cell (tCAR-T), is a T cell with a single chimeric antigen polypeptide comprising two distinct extracellular ligand-binding (antigen/protein recognition) domains capable of interacting with two different cell surface molecules (e.g., antigen/protein), wherein the extracellular ligand-binding domains are linked together by one or more flexible linkers and share one or more costimulatory domains, wherein the binding of the first or second extracellular ligand-binding domain will signal through one or more the costimulatory domains(s) and a signaling transducing domain.

In certain embodiments, the T cell is deficient in one or more antigens or cell surface proteins (e.g., CD7 and CD2 for a CD7*CD2-tCARΔCD7ΔCD2 cell, or CD2 for a CD3*CD2-tCARΔCD3ΔCD2 cell). In non-limiting examples, the deficiency in the antigen(s) or cell surface protein(s) resulted from (a) modification of antigen or cell surface protein expressed by the T cell such that the chimeric antigen receptor no longer specifically binds the modified antigen(s) or cell surface protein(s) (e.g., the epitope of the one or more antigens recognized by the chimeric antigen receptor may be modified by one or more amino acid changes (e.g., substitutions or deletions) or the epitope may be deleted from the antigen), (b) modification of the T cell such that expression of antigen(s) or cell surface protein(s) is/are reduced in the T cell by at least 50%, at least 60%, at least 70%, at least 80%, at least 90% or more, or (c) modification of the T cell such that antigen(s) or cell surface protein(s) is/are not expressed (e.g., by deletion or disruption of the gene encoding antigen or cell surface protein). In each of the above embodiments, the CAR-T cell may be deficient in one or preferably all the antigens or cell surface proteins to which the chimeric antigen receptor specifically binds. The methods to genetically modify a T cell to be deficient in one or more antigens or cell surface proteins are well known in art and non-limiting examples are provided herein. In embodiments described below, the CRISPR-Cas9 system is used to modify a T cell to be deficient in one or more antigen(s) or cell surface protein(s). Any of these may be accomplished by the methods disclosed herein. In further embodiments, the T cell comprises a suicide gene.

A tCAR for a genome-edited, tandem CAR-T cell, i.e., CD2*CD3-tCARTΔCD2ΔCD3ε, may be generated by cloning a commercially synthesized anti-CD2 single chain variable fragment (scFv) and an anti-CD3 single chain variable fragment (scFv), separated by a peptide linker, into a lentiviral vector containing, e.g., a 2^(nd) or 3^(rd) generation CAR backbone with CD28 and/or 4-1BB internal signaling domains. An extracellular hCD34 domain may be added after a P2A peptide to enable both detection of CAR following viral transduction and purification using anti-hCD34 magnetic beads. A similar method may be followed for making tCARs specific for other malignant T cell antigens.

Tandem CARs may have different linker structures, i.e., be linear or hairpin, and the hairpin linker may optionally comprise a (Cys=Cys) double-stranded bond (DSB).

A linear tandem CAR-T cell comprises a chimeric antigen receptor (CAR) polypeptide comprising a first signal peptide, a first extracellular ligand-binding domain, a second extracellular ligand-binding domain, a hinge region, a transmembrane domain, one or more co-stimulatory domains, and a signaling transducing domain, wherein the first extracellular ligand-binding antigen recognition domain and the second extracellular ligand-binding antigen recognition domain have affinities for different cell surface molecules, i.e., antigens on a cancer cell, for example, a malignant T cell, B cell, or plasma cell; and wherein the linear tandem CAR-T cell possesses one or more genetic modifications, deletions, or disruptions resulting in reduced expression of the cell surface molecules in the linear tandem CAR-T cell.

In another embodiment, the signal peptide is the signal peptide from human CD8α.

In a third embodiment, the first extracellular ligand-binding domain comprises a single chain antibody fragment (scFv), comprising the light (V_(L)) and the heavy (V_(H)) variable fragment, designated V_(H)1 and V_(L)1 and joined by a linker (e.g., GGGGS (SEQ ID NO: 3065)). In some embodiments, this linker peptide is repeated 2, 3, 4, 5 or 6 times. In some embodiments. the first antigen recognition domain can be selected from: 1) V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1 or 2) V_(L)1—(GGGGS)₄ (SEQ ID NO: 3066)—V_(H)1.

In some embodiments, the second extracellular ligand-binding domain comprises a single chain antibody fragment (scFv), comprising the light (V_(L)) and the heavy (V_(H)) variable fragment, designated V_(H)2 and V_(L)2 and joined by a linker (e.g., GGGGS (SEQ ID NO: 3065)). In some embodiments, this linker peptide is repeated 2, 3, 4, 5 or 6 times. In some embodiments, the first antigen recognition domain can be selected from: 1) V_(H)2-(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)2 or 2) V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2.

In further embodiments, the first antigen recognition domain and second antigen recognition domain are connected by a short linker peptide of 5 amino acids (GGGGS (SEQ ID NO: 3065)). In some embodiments, this linker peptide is repeated 2, 3, 4, 5, or 6 times.

Tandem CAR Constructs

In one embodiment, the first extracellular ligand-binding domain antigen recognition comprises a single chain antibody fragment (scFv), comprising the heavy (V_(H)) and the light (V_(L)) variable fragment, designated V_(H)1 and V_(L)1, and joined by a linker (e.g., GGGGS (SEQ ID NO: 3065)), targets a cell surface molecule, i.e., an antigen expressed on a malignant cell.

In certain embodiments, the heavy (V_(H)) and the light (V_(L)) variable fragment, designated V_(H)1 and V_(L)1, targeting an antigen expressed on a malignant T cell is selected from BCMA, CS1, CD38, CD138, CD19, CD33, CD123, CD371, CD117, CD135, Tim-3, CD5, CD7, CD2, CD4, CD3, CD79A, CD79B, APRIL, CD56, and CD1a.

In certain embodiments, the second extracellular ligand-binding domain antigen recognition comprises a single chain antibody fragment (scFv), comprising the heavy (V_(H)) and the light (V_(L)) variable fragment, designated V_(H)2 and V_(L)2, and joined by a linker (e.g., GGGGS (SEQ ID NO: 3065)), and targets a cell surface molecule, i.e., an antigen, expressed on a malignant cell.

In certain embodiments, the heavy (V_(H)) and the light (V_(L)) variable fragments, designated V_(H)2 and V_(L)2, targeting an antigen expressed on a malignant T cell is selected from BCMA, CS1, CD38, CD138, CD19, CD33, CD123, CD371, CD117, CD135, Tim-3, CD5, CD7, CD2, CD4, CD3, CD79A, CD79B, APRIL, CD56, and CD1a and differs from the variable heavy (V_(H)1) and light sequences (V_(L)1) of the first extracellular ligand-binding domain of the CAR molecule.

Additional examples of tandem CARs are given below in Table 5.

TABLE 5 Tandem CARs and CAR-Ts Example Antigen Target CAR-T cell Antigen Deletion/Suppression T1 APRILxBCMA — T2 APRILxCD19 — T3 APRILxCD38 — T4 APRILxCD38 CD38 T5 APRILxCS1 — T6 APRILxCS1 CS1 T7 BCMAxCD19 — T8 BCMAxCD38 — T9 BCMAxCD38 CD38 T10 BCMAxCS1 — T11 BCMAxCS1 CS1 T12 CD138xAPRIL T13 CD138xBCMA T14 CD138xCD19 T15 CD138xCD38 T16 CD138xCD38 CD38 T17 CD138xCD79A T18 CD138xCD79B T19 CD138xCS1 T20 CD138xCS1 CS1 T21 CD19xCD38 — T22 CD19xCD38 CD38 T23 CD2xCD3ε — T24 CD2xCD3ε CD2 T25 CD2xCD3ε CDε T26 CD2xCD3ε CD2 and CD3ε T27 CD2xCD4 — T28 CD2xCD4 CD2 T29 CD2xCD4 CD4 T30 CD2xCD4 CD2 and CD4 T31 CD2xCD4 CD2 and TRAC T32 CD2xCD4 CD4 and TRAC T33 CD2xCD4 CD2 and CD4 and TRAC T34 CD2xCD5 — T35 CD2xCD5 CD2 T36 CD2xCD5 CD5 T37 CD2xCD5 CD2 and CD5 T38 CD2xCD5 CD2 and TRAC T39 CD2xCD5 CD5 and TRAC T40 CD2xCD5 CD2 and CD5 and TRAC T41 CD2xCD7 — T42 CD2xCD7 CD2 T43 CD2xCD7 CD7 T44 CD2xCD7 CD2 and CD7 T45 CD2xCD7 CD2 and TRAC T46 CD2xCD7 CD7 and TRAC T47 CD2xCD7 CD2 and CD7 and TRAC T48 CD3εxCD4 — T49 CD3εxCD4 CD3ε T50 CD3εxCD4 CD4 T51 CD3εxCD4 CD3ε and CD4 T52 CD3εxCD5 — T53 CD3εxCD5 CD3ε T54 CD3εxCD5 CD5 T55 CD3εxCD5 CD3ε and CD5 T56 CD3εxCD7 — T57 CD3εxCD7 CD3ε T58 CD3εxCD7 CD7 T59 CD3εxCD7 CD3ε and CD7 T60 CD4xCD5 — T61 CD4xCD5 CD4 T62 CD4xCD5 CD5 T63 CD4xCD5 CD4 and CD5 T64 CD4xCD5 CD4 and TRAC T65 CD4xCD5 CD5 and TRAC T66 CD4xCD5 CD4 and CD5 and TRAC T67 CD4xCD7 — T68 CD4xCD7 CD4 T69 CD4xCD7 CD7 T70 CD4xCD7 CD4 and CD7 T71 CD4xCD7 CD4 and TRAC T72 CD4xCD7 CD4 and TRAC T73 CD4xCD7 CD4 and CD7 and TRAC T74 CD5xCD7 — T75 CD5xCD7 CD5 T76 CD5xCD7 CD7 T77 CD5xCD7 CD5 and CD7 T78 CD5xCD7 CD5 and TRAC T79 CD5xCD7 CD7 and TRAC T80 CD5xCD7 CD5 and CD7 and TRAC T81 CD79AxAPRIL T82 CD79AxBCMA T83 CD79AxCD19 T84 CD79AxCD38 T85 CD79AxCD38 CD38 T86 CD79AxCD79B T87 CD79AxCS1 T88 CD79AxCS1 CS1 T89 CD79BxAPRIL T90 CD79BxBCMA T91 CD79BxCD19 T92 CD79BxCD38 T93 CD79BxCD38 CD38 T94 CD79BxCD79A T95 CD79BxCS1 T96 CD79BxCS1 CS1 T97 CS1xCD19 — T98 CS1xCD19 CS1 T99 CS1xCD38 — T100 CS1xCD38 CS1 T101 CS1xCD38 CD38 T102 CS1xCD38 CS1 and CD38 T103 TCRβxCD2 — T104 TCRβxCD2 TCRβ T105 TCRβxCD2 CD2 T106 TCRβxCD2 TCRβ and CD2 T107 TCRβxCD3ε T108 TCRβxCD3ε TCRβ T109 TCRβxCD3ε CDε T110 TCRβxCD3ε TCRβ and CD3ε T111 TCRβxCD4 — T112 TCRβxCD4 TCRβ T113 TCRβxCD4 CD4 T114 TCRβxCD4 TCRβ and CD4 T115 TCRβxCD5 — T116 TCRβxCD5 TCRβ T117 TCRβxCD5 CD5 T118 TCRβxCD5 TCRβ and CD5 T119 TCRβxCD7 — T120 TCRβxCD7 TCRβ T121 TCRβxCD7 CD7 T122 TCRβxCD7 TCRβ and CD7 T123 TRACxCD2 — T124 TRACxCD2 TRAC T125 TRACxCD2 CD2 T126 TRACxCD2 TRAC and CD2 T127 TRACxCD3ε — T128 TRACxCD3ε TRAC T129 TRACxCD3ε CDε T130 TRACxCD3ε TRAC and CD3ε T131 TRACxCD4 — T132 TRACxCD4 TRAC T133 TRACxCD4 CD4 T134 TRACxCD4 TRAC and CD4 T135 TRACxCD5 — T136 TRACxCD5 TRAC T137 TRACxCD5 CD5 T138 TRACxCD5 TRAC and CD5 T139 TRACxCD7 — T140 TRACxCD7 TRAC T141 TRACxCD7 CD7 T142 TRACxCD7 TRAC and CD7

In some embodiments, hairpin tandem CAR constructs may be provided herein, such as including, but not limited to, a construct incorporating the V_(H) and V_(L) domains of CD2 and CD3 scFvs (Table 6).

TABLE 6 Hairpin Tandem CAR Constructs Targeting CD2 and CD3. Clone 5 Clone 6 Clone 7 Clone 8 Clone 13 Clone 14 Clone 15 Clone 16 CD8a CD8a CD8a CD8a CD8a CD8a CD8a CD8a CD3-V_(L) CD3-V_(L) CD3-V_(L) CD3-V_(L) CD2-V_(L) CD2-V_(L) CD3-V_(L) CD3-V_(L) GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) CD2-V_(L) CD2-V_(L) CD2-V_(L) CD2-V_(L) CD3-V_(L) CD3-V_(L) CD2-V_(L) CD2-V_(L) (GGGGS)₁₀ (GGGGS)₄ (GGGG (GGG (GGG (GGGGS (GGGG (GGGG (SEQ GGGG S)₁₀ GS)₄G GS)₁₀ )₄GGGG S)₁₀ S)₄GGGG ID NO: P(GGGG (SEQ GGGP(G (SEQ P(GGGG (SEQ P(GGGG 3067) S)₄ ID NO:  GGGS)₄  ID NO:  S)₄  ID NO:  S)₄  (SEQ 3067) (SEQ 3067) (SEQ 3067) (SEQ ID NO:  ID NO:  ID NO:  ID NO:  3068) 3068) 3068) 3068) CD2-V_(H) CD2-V_(H) CD2-V_(H) CD2-V_(H) CD3-V_(H) CD3-V_(H) CD2-V_(H) CD2-V_(H) GGGGS₄ GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 GGGGS4 (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) NO: 9) CD3-V_(H) CD3-V_(H) CD3-V_(H) CD3-V_(H) CD2-V_(H) CD2-V_(H) CD3-V_(H) CD3-V_(H) CD28 CD28 CD28 CD28 CD28 CD28 CD28 CD28 Tm Tm Tm Tm Tm Tm Tm Tm CD28 CD28 CD28 CD28 CD28 CD28 CD28 CD28 CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ CD3z₍₁₋₂₎ P2A P2A P2A P2A P2A P2A P2A P2A CD34 CD34 CD34 CD34 CD34 CD34 CD34 CD34

Dual CAR-T Cells

In certain embodiments, the disclosure provides an engineered T cell with two distinct chimeric antigen receptor polypeptides with affinity to different antigen(s) or cell surface protein(s) expressed within the same effector cell, wherein each CAR functions independently. The CAR may be expressed from single or multiple polynucleotide sequences that specifically bind different antigen(s) or cell surface protein(s), wherein the T cell is deficient in the antigen(s) or cell surface protein(s) to which the CARs bind (e.g., CD7*CD2-dCARΔCD7ΔCD2 cell). In non-limiting examples, the deficiency in the antigen(s) or cell surface protein(s) resulted from (a) modification of antigen or cell surface protein expressed by the T cell such that the chimeric antigen receptor no longer specifically binds the modified antigen(s) or cell surface protein(s) (e.g., the epitope of the one or more antigens recognized by the chimeric antigen receptor may be modified by one or more amino acid changes (e.g., substitutions or deletions) or the epitope may be deleted from the antigen), (b) modification of the T cell such that expression of antigen(s) or cell surface protein(s) is/are reduced in the T cell by at least 50%, at least 60%, at least 70%, at least 80%, at least 90% or more, or (c) modification of the T cell such that antigen(s) or cell surface protein(s) is/are not expressed (e.g., by deletion or disruption of the gene encoding antigen or cell surface protein). In each of the above embodiments, the CAR-T cell may be deficient in one or preferably all the antigens or cell surface proteins to which the chimeric antigen receptor specifically binds. The methods to genetically modify a T cell to be deficient in one or more antigens or cell surface proteins are well known in art and non-limiting examples are provided herein. In embodiments described below, the CRISPR-Cas9 system is used to modify a T cell to be deficient in one or more antigen(s) or cell surface protein(s). Any of these may be accomplished by the methods disclosed herein. In further embodiments, the T cell comprises a suicide gene.

A dCAR for a genome-edited, dual CAR-T cell, i.e., CD2*CD38-dCARTΔCD2ΔCD3ε, may be generated by cloning a commercially synthesized anti-CD2 single chain variable fragment into a lentiviral vector containing, e.g., a 2^(nd) or 3^(rd) generation CAR backbone with CD28 and/or 4-1BB internal signaling domains and cloning a commercially synthesized anti-CD38 single chain variable into the same lentiviral vector containing an additional 2^(nd) or 3^(rd) generation CAR backbone with CD28 and/or 4-1BB internal signaling domains resulting in a plasmid from which the two CAR constructs are expressed from the same vector. An extracellular hCD34 domain may be added after a P2A peptide to enable both detection of CAR following viral transduction and purification using anti-hCD34 magnetic beads. A similar method may be followed for making tCARs specific for other malignant T cell antigens.

In a similar manner, other dual CARs may be constructed and are given below in Tables 5-7.

In one embodiment, a dual CAR-T cell comprises (i) a first chimeric antigen receptor (CAR) polypeptide comprising a first signal peptide, a first antigen recognition domain, a first hinge region, a first transmembrane domain, a first co-stimulatory domain, and a first signaling domain; and (ii) a second chimeric antigen receptor polypeptide comprising a second signaling peptide, a second antigen recognition domain, a second hinge region, a second transmembrane domain, a second co-stimulatory domain, and a second signaling domain; wherein the first antigen recognition domain and the second antigen recognition domain have affinities for different target antigens; and wherein the dual CAR-T cell possesses one or more genetic disruptions resulting in reduced expression of the target antigen in the dual CAR-T cell.

In a second embodiment, the first signal peptide is a CD8a signal sequence.

In a third embodiment, the first antigen recognition domain is fusion protein of the variable regions of immunoglobulin heavy and light chains, designated V_(H)1 and V_(L)1, for the first antigen recognition domain, connected by a short linker peptide of 5 amino acids (GGGGS (SEQ ID NO: 3065)). In some embodiments, this linker peptide is repeated 3 or 4 times. In some embodiments, the first antigen recognition domain can be selected from V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1 or V_(L)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1.

In some embodiments, the first hinge region comprises CD8a.

In some embodiments, the first transmembrane domain is CD8 or CD28.

In some embodiments, the first co-stimulatory domain comprises 4-1BB, CD28, or a combination of both, in either order, i.e., 4-1BB-CD28 or CD28-4-1BB.

In some embodiments, the first signaling domain is CD3ζ or a CD3ζ bi-peptide, i.e., CD3ζ-CD3ζ.

In some embodiments, the second signal peptide is a CD8a signal sequence of SEQ NO: 1.

In some embodiments, the second antigen recognition domain is fusion protein of the variable regions of immunoglobulin heavy and light chains, designated V_(H)2 and V_(L)2, for the second antigen recognition domain, connected by a short linker peptide of 5 amino acids (GGGGS (SEQ ID NO: 3065)). In some embodiments, this linker peptide is repeated 3 or 4 times. In some embodiments, the second antigen recognition domain can be selected from V_(H)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)2 or V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1

In some embodiments, the second hinge region comprises CD8a.

In some embodiments, the second transmembrane domain is CD8 or CD28.

In some embodiments, the second co-stimulatory domain comprises 4-1BB, CD28, or a combination of both, in either order, i.e., 4-1BB-CD28 or CD28-4-1BB.

In some embodiments, the second signaling domain is CD3ζ or a CD3ζ bi-peptide, i.e., CD3ζ-CD3ζ.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1 and a second antigen recognition domain fusion protein of V_(H)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2,

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(L)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1 and a second antigen recognition domain fusion protein of V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)2 and a second antigen recognition domain fusion protein of V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2 and a second antigen recognition domain fusion protein of V_(L)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1 and a second antigen recognition domain fusion protein of V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(L)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1 and a second antigen recognition domain fusion protein of V_(H)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)2.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(H)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)2 and a second antigen recognition domain fusion protein of V_(L)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)1.

In some embodiments, the CAR polypeptide comprises a first antigen recognition domain fusion protein of V_(L)2—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(H)2 and a second antigen recognition domain fusion protein of V_(H)1—(GGGGS)₃₋₄ (SEQ ID NO: 3066)—V_(L)1.

In some embodiments, the CAR polypeptide comprises at least one high efficiency cleavage site, wherein the high efficiency cleavage site is selected from P2A, T2A, E2A, and F2A.

In some embodiments, the CAR polypeptide comprises a suicide gene.

In some embodiments, the CAR polypeptide comprises a mutant cytokine receptor.

In some embodiments, the dual CAR-T cell targets two antigens selected from CD5, CD7, CD2, CD4, CD3, CD33, CD123 (IL3RA), CD371 (CLL-1; CLEC12A), CD117 (c-kit), CD135 (FLT3), BCMA, CS1, CD38, CD79A, CD79B, CD138, and CD19, APRIL, and TACI.

Additional examples of dual CARs are given below in Table 7.

TABLE 7 Dual CARs and dCAR-Ts Antigen Targets of Example CARs in dCAR-T cell Antigen Deletion/Suppression D1 APRILxBCMA — D2 APRILxCD19 — D3 APRILxCD38 — D4 APRILxCD38 CD38 D5 APRILxCS1 — D6 APRILxCS1 CS1 D7 BCMAxCD19 — D8 BCMAxCD38 — D9 BCMAxCD38 CD38 D10 BCMAxCS1 D11 BCMAxCS1 CS1 D12 CD138xAPRIL D13 CD138xBCMA D14 CD138xCD19 D15 CD138xCD38 D16 CD138xCD38 CD38 D17 CD138xCD79A D18 CD138xCD79B D19 CD138xCS1 D20 CD138xCS1 CS1 D21 CD19xCD38 — D22 CD19xCD38 CD38 D23 CD2xCD3ε — D24 CD2xCD3ε CD2 D25 CD2xCD3ε CD3ε D26 CD2xCD3ε CD2 and CD3ε D27 CD2xCD4 — D28 CD2xCD4 CD2 D29 CD2xCD4 CD4 D30 CD2xCD4 CD2 and CD4 D31 CD2xCD4 CD2 and TRAC D32 CD2xCD4 CD4 and TRAC D33 CD2xCD4 CD2 and CD4 and TRAC D34 CD2xCD5 — D35 CD2xCD5 CD2 D36 CD2xCD5 CD5 D37 CD2xCD5 CD2 and CD5 D38 CD2xCD5 CD2 and TRAC D39 CD2xCD5 CD5 and TRAC D40 CD2xCD5 CD2 and CD5 and TRAC D41 CD2xCD7 — D42 CD2xCD7 CD2 D43 CD2xCD7 CD7 D44 CD2xCD7 CD2 and CD7 D45 CD2xCD7 CD2 and TRAC D46 CD2xCD7 CD7 and TRAC D47 CD2xCD7 CD2 and CD7 and TRAC D48 CD3εxCD4 — D49 CD3εxCD4 CD3ε D50 CD3εxCD4 CD4 D51 CD3εxCD4 CD3ε and CD4 D52 CD3εxCD5 — D53 CD3εxCD5 CD3ε D54 CD3εxCD5 CD5 D55 CD3εxCD5 CD3ε and CD5 D56 CD3εxCD7 — D57 CD3εxCD7 CD3ε D58 CD3εxCD7 CD7 D59 CD3εxCD7 CD3ε and CD7 D60 CD4xCD5 — D61 CD4xCD5 CD4 D62 CD4xCD5 CD5 D63 CD4xCD5 CD4 and CD5 D64 CD4xCD5 CD4 and TRAC D65 CD4xCD5 CD5 and TRAC D66 CD4xCD5 CD4 and CD5 and TRAC D67 CD4xCD7 — D68 CD4xCD7 CD4 D69 CD4xCD7 CD7 D70 CD4xCD7 CD4 and CD7 D71 CD4xCD7 CD4 and TRAC D72 CD4xCD7 CD7 and TRAC D73 CD4xCD7 CD4 and CD7 and TRAC D74 CD5xCD7 — D75 CD5xCD7 CD5 D76 CD5xCD7 CD7 D77 CD5xCD7 CD5 and CD7 D78 CD5xCD7 CD5 and TRAC D79 CD5xCD7 CD7 and TRAC D80 CD5xCD7 CD5 and CD7 and TRAC D81 CD79AxAPRIL D82 CD79AxBCMA D83 CD79AxCD19 D84 CD79AxCD38 D85 CD79AxCD38 CD38 D86 CD79AxCD79B D87 CD79AxCS1 D88 CD79AxCS1 CS1 D89 CD79BxAPRIL D90 CD79BxBCMA D91 CD79BxCD19 D92 CD79BxCD38 D93 CD79BxCD38 CD38 D94 CD79BxCD79A D95 CD79BxCS1 D96 CD79BxCS1 CS1 D97 CS1xCD19 — D98 CS1xCD19 CS1 D99 CS1xCD38 — D100 CS1xCD38 CS1 D101 CS1xCD38 CD38 D102 CS1xCD38 CS1 and CD38 D103 TCRβxCD2 — D104 TCRβxCD2 TCRβ D105 TCRβxCD2 CD2 D106 TCRβxCD2 TCRβ and CD2 D107 TCRβxCD3ε — D108 TCRβxCD3ε TCRβ D109 TCRβxCD3ε CD3ε D110 TCRβxCD3ε TCRβ and CD3ε D111 TCRβxCD4 — D112 TCRβxCD4 TCRβ D113 TCRβxCD4 CD4 D114 TCRβxCD4 TCRβ and CD4 D115 TCRβxCD5 — D116 TCRβxCD5 TCRβ D117 TCRβxCD5 CD5 D118 TCRβxCD5 TCRβ and CD5 D119 TCRβxCD7 — D120 TCRβxCD7 TCRβ D121 TCRβxCD7 CD7 D122 TCRβxCD7 TCRβ and CD7 D123 TRACxCD2 — D124 TRACxCD2 TRAC D125 TRACxCD2 CD2 D126 TRACxCD2 TRAC and CD2 D127 TRACxCD3ε — D128 TRACxCD3ε TRAC D129 TRACxCD3ε CDε D130 TRACxCD3ε TRAC and CD3ε D131 TRACxCD4 — D132 TRACxCD4 TRAC D133 TRACxCD4 CD4 D134 TRACxCD4 TRAC and CD4 D135 TRACxCD5 — D136 TRACxCD5 TRAC D137 TRACxCD5 CD5 D138 TRACxCD5 TRAC and CD5 D139 TRACxCD7 — D140 TRACxCD7 TRAC D141 TRACxCD7 CD7 D142 TRACxCD7 TRAC and CD7

Cytokine/Chemokine/Transcription Factor Gene Deletion or Suppression

Cytokine release syndrome (CRS) is caused by a large, rapid release of cytokines from immune cells in response to immunotherapy (or other immunological stimulus). Accordingly, reducing the level of cytokines released would prevent or reduce the development and/or maintenance of CRS. As disclosed herein, this can be accomplished by modifying, disrupting, or deleting one or more cytokine/chemokine/transcription factor genes. One method to accomplish this is genetic ablation (gene silencing) in which gene expression is abolished through the alteration or deletion of genetic sequence information. This can be accomplished using known genetic engineering tools in the art such as Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), CRISPR, and also by transfection of small interfering RNAs (siRNAs).

Another technique is expression of an scFv with an endoplasmic reticulum (ER) binding tether to bind the cytokine in the ER and prevent secretion. Specific constructs, named protein expression blockers (PEBLs), prevent transport of targeted proteins to the cell membrane. PEBL constructs can be readily combined with other gene modification systems for ex vivo cell processing of immune cells. A short hairpin RNA or small hairpin RNA (shRNA/Hairpin Vector) is an artificial RNA molecule with a tight hairpin turn that can be used to silence target gene expression, i.e., of antigens, via RNA interference (RNAi). Expression of shRNA in cells is typically accomplished by delivery of plasmids or through viral or bacterial vectors.

Cytokines or chemokines that can be deleted from immune effector cells as disclosed herein, e.g., by targeted transduction of a CAR into the gene sequence of the cytokine, include without limitation the following: XCL1, XCL2, CCL1, CCL2, CCL3, CCL4, CCL5, CCL7, CCL8, CCL11, CCL13, CCL14, CCL15, CCL16, CCL17, CCL18, CCL19, CCL20, CCL21, CCL22, CCL23, CCL24, CCL25, CCL26, CCL27, CXCL1, CXCL2, CXCL3, CXCL4, CXCL5, CXCL6, CXCL7, CXCL8, CXCL9, CXCL10, CXCL11, CXCL12, CXCL13, CXCL14, CX3CL1, IL-1α, IL-1β, IL-1RA, IL-18, IL-2, IL-4, IL-7, IL-9, IL-13, IL-15, IL-3, IL-5, GM-CSF, IL-6, IL-11, G-CSF, IL-12, LIF, OSM, IL-10, IL-20, IL-14, IL-16, IL-17, IFN-α, IFN-β, IFN-γ, CD154, LT-β, TNF-α, TNF-β, 4-1BBL, APRIL, CD70, CD153, CD178, GITRL, LIGHT, OX40L, TALL-1, TRAIL, TWEAK, TRANCE, TGF-β1, TGF-β2, TGF-β3, Epo, Tpo, Flt-3L, SCF, M-CSF, MSP, A2M, ACKR1, ACKR2, ACKR3, ACVR1, ACVR2B, ACVRL1, ADIPOQ, AGER, AGRN, AIMP1, AREG, BMP1, BMP10, BMP15, BMP2, BMP3, BMP4, BMP5, BMP6, BMP7, BMP8A, BMP8B, BMPR2, C10 orf99, C1 QTNF4, C5, CCL28, CCR1, CCR2, CCR3, CCR5, CCR6, CCR7, CD109, CD36, CD4, CD40LG, CD74, CER1, CHRD, CKLF, CLCF1, CMTM1, CMTM2, CMTM3, CMTM4, CMTM5, CMTM6, CMTM7, CMTM8, CNTF, CNTFR, COPS5, CRLF1, CSF1, CSF1R, CSF2, CSF3, CSF3R, CTF1, CX3CR1, CXCL16, CXCL17, CXCR1, CXCR2, CXCR3, CXCR4, CXCR6, EBI3, EDN1, ELANE, ENG, FAM3B, FAM3C, FAM3D, FAS, FASLG, FGF2, FLT3LG, FZD4, GBP1, GDF1, GDF10, GDF11, GDF15, GDF2, GDF3, GDF5, GDF6, GDF7, GDF9, GPI, GREM1, GREM2, GRN, HAX1, HFE2, HMGB1, HYAL2, IFNA10, IFNA14, IFNA16, IFNA2, IFNA5, IFNA6, IFNA8, IFNAR1, IFNAR2, IFNB1, IFNE, IFNG, IFNGR1, IFNK, IFNL1, IFNL3, IFNW1, IL10RA, IL11RA, IL12A, IL12B, IL12RB1, IL17A, IL17B, IL17C, IL17D, IL17F, IL18BP, IL-19, IL1F10, IL1R1, IL1R2, IL1 RAPL1, IL1RL1, IL1RN, IL20RA, IL20RB, IL21, IL22, IL22RA1, IL22RA2, IL23A, IL23R, IL24, IL25, IL26, IL27, IL2RA, IL2RB, IL2RG, IL31, IL31RA, IL32, IL33, IL34, IL36A, IL36B, IL36G, IL36RN, IL37, IL6R, IL6ST, INHA, INHBA, INHBB, INHBC, INHBE, ITGA4, ITGAV, ITGB1, ITGB3, KIT, KITLG, KLHL20, LEFTY1, LEFTY2, LIFR, LTA, LTB, LTBP1, LTBP3, LTBP4, MIF, MINOS1-, MSTN, NAMPT, NBL1, NDP, NLRP7, NODAL, NOG, NRG1, NRP1, NRP2, OSMR, PARK7, PDPN, PF4, PF4V1, PGLYRP1, PLP2, PPBP, PXDN, SCG2, SCGB3A1, SECTM1, SLURP1, SOSTDC1, SP100, SPP1, TCAP, TGFBR1, TGFBR2, TGFBR3, THBS1, THNSL2, THPO, TIMP1, TNF, TNFRSF11, TNFRSF1A, TNFRSF9, TNFRSF10, TNFSF11, TNFSF12, TNFSF12-, TNFSF13, TNFSF13B, TNFSF14, TNFSF15, TNFSF18, TNFSF4, TNFSF8, TNFSF9, TRIM16, TSLP, TWSG1, TXLNA, VASN, VEGFA, VSTM1, WFIKKN1, WFIKKN2, WNT1, WNT2, WNT5A, WNT7A, and ZFP36.

In some embodiments, the cytokine is chosen from cytokine is chosen from MCP1 (CCL2), MCP-2, GM-CSF, G-CSF, M-CSF, Il-4, and IFNγ.

In certain embodiments, transcription factors that can be deleted from immune effector cells as disclosed herein include AHR, BCL6, FOXP3, GATA3, MAF, RORC, SPI1, and TBX21.

The sequences of these genes are known and available in the art and can include, for example, those provided in Table 10.

Selection of Priority Target Genes

Cytokine/chemokine gene targets of specific interest for deletion or suppression (e.g., ablation, knock-out, KO) in CAR-T cells for the mitigation of CRS have been categorized into groups based on biological function. CRS development is dependent upon CAR-T cell activation and subsequent cytokine release, which initiates a dysregulated immune system in the recipient of the CAR-T cell therapy. Several studies have indicated that recipient myeloid activation is necessary for the development of CRS.

The first group of potential genes to KO in CAR-T are surface receptors that, when engaged with myeloid cells in normal immunological responses activate the myeloid cells (e.g., CD40L). The second group are cytokines that are released from CAR-T cells that activate myeloid cells (e.g., GM-CSF). In both these categories, the goal is to prevent CAR-T cell signaling, which will activate recipient myeloid cells and initiate CRS.

The third category of targets are endogenous T cell receptors that increase T cell activation (potentially in the absence of tumor target) that are integrated into the CAR-T receptor (e.g., endogenous CD28). The aim is to curtail activation of the CAR-T from non-tumor interactions, such as activated myeloid cells that could engage with CD28 on activated T cells, thus amplifying T cell cytokine production and subsequent myeloid activation.

The fourth and fifth categories of gene KO targets are transcription factors and cytokines that drive CAR-T cell differentiation and subsequent functional characteristics. CAR-T cells that are phenotypically similar to normal cytotoxic T cells (CTL, typically identified by CD8 expression) are capable of direct tumor killing through T cell mediated effector functions. CTL are supported and maintained by T helper cells (expressing CD4). Importantly, subsets of T helper cells can support CTL (i.e., Th1 cells) or inhibit (i.e., Th2 cells). Other T cells, such as Tregs can also inhibit CTL development and function. The aim is to target cytokines or transcription factors in the CAR-T population that would lead to CAR-T differentiation into non-cytotoxic T cell populations. Additionally, Th2 cells produce cytokines (such as GM-CSF and IL-4), which are indicative markers of CRS. It is likely that CAR-T phenotypes, which cannot optimally kill tumor cells, will be activated via CAR-T receptors, produce signals that drive CRS in the host, increase the time required for tumor killing, and require higher CAR-T cell doses than optimized “killing” products. Thus, knocking out or ablating (or suppressing) transcription factors (such as GATA3) or cytokines (such as IL-4) will prevent (or reduce) Th2 bias and reduce CRS.

Of additional interest regarding both myeloid activating cytokines and optimized CAR-T cell differentiation is the potential to mitigate CAR-T neurotoxicity. Neurotoxicity occurs in a small population of CAR-T recipients with CRS. Research has shown that CRS patients that progress to develop neurotoxicity have increased IL-5 and ferritin levels (Santomasso et al., 2017 and Philip et al., 2019). These two biomarkers indicate that mast cell activation may be involved with CNS complications. IL-5 is a key cytokine produced by Th2 cells, eosinophils and mast cells. Excessive levels of ferritin are observed in mastocytosis and several diseases involving mast cell dysregulation. Additionally, many mast cell diseases include neurological dysregulation. Given raised levels of IL-5, ferritin, and neurological toxicity in some patients, reducing mast cell activation by cytokines such as IL-5, or preventing Th2 cell development which drives IL-5-dependent mast cell activation, may also mitigate neurological complications seen in CRS recipients. With respect to CNS complications, CX3CR1 and OX40 were also highlighted, due to previously demonstrated high T cell burden in the CNS. CX3CR1 is a T cell chemokine receptor that principally directs T cells and potentially CAR-T cells into the CNS. OX40 is the T cell receptor which facilitates activation by cell-cell interaction with OX40L on eosinophils and mast cells.

Thus, in certain embodiments, the cytokine is chosen from CCL2 (MCP1), MCP-2, GM-CSF, G-CSF, M-CSF, Il-4, and IFNγ.

Indications and Standards of Care in CAR-T Therapy

In some embodiment, the genome-edited immune effector cells disclosed herein, and/or generated using the methods disclosed herein, express one or more chimeric antigen receptors (CARs) and can be used as a medicament, i.e., for the treatment of disease. In many embodiments, the cells are CAR-T cells.

Cells disclosed herein, and/or generated using the methods disclosed herein, may be used in immunotherapy and adoptive cell transfer, for the treatment, or the manufacture of a medicament for treatment, of cancers, autoimmune diseases, infectious diseases, and other conditions.

The cancer may be a hematologic malignancy or solid tumor. Hematologic malignancies include leukemias, lymphomas, multiple myeloma, and subtypes thereof. Lymphomas can be classified various ways, often based on the underlying type of malignant cell, including Hodgkin's lymphoma (often cancers of Reed-Sternberg cells, but also sometimes originating in B cells; all other lymphomas are non-Hodgkin's lymphomas), B-cell lymphomas, T-cell lymphomas, mantle cell lymphomas, Burkitt's lymphoma, follicular lymphoma, and others as defined herein and known in the art.

B-cell lymphomas include, but are not limited to, diffuse large B-cell lymphoma (DLBCL), chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL), and others as defined herein and known in the art.

T-cell lymphomas include T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), peripheral T-cell lymphoma (PTCL), T-cell chronic lymphocytic leukemia (T-CLL) Sezary syndrome, and others as defined herein and known in the art.

Leukemias include Acute myeloid (or myelogenous) leukemia (AML), chronic myeloid (or myelogenous) leukemia (CML), acute lymphocytic (or lymphoblastic) leukemia (ALL), chronic lymphocytic leukemia (CLL) hairy cell leukemia (sometimes classified as a lymphoma), and others as defined herein and known in the art.

Plasma cell malignancies include lymphoplasmacytic lymphoma, plasmacytoma, and multiple myeloma.

In some embodiments, the medicament can be used for treating cancer in a patient, particularly for the treatment of solid tumors such as melanomas, neuroblastomas, gliomas or carcinomas such as tumors of the brain, head and neck, breast, lung (e.g., non small cell lung cancer, NSCLC), reproductive tract (e.g., ovary), upper digestive tract, pancreas, liver, renal system (e.g., kidneys), bladder, prostate and colorectum.

In another embodiment, the medicament can be used for treating cancer in a patient, particularly for the treatment of hematologic malignancies selected from multiple myeloma and acute myeloid leukemia (AML) and for T-cell malignancies selected from T-cell acute lymphoblastic leukemia (T-ALL), non-Hodgkin's lymphoma, and T-cell chronic lymphocytic leukemia (T-CLL).

In some embodiments, the cells may be used in the treatment of autoimmune diseases such as lupus, autoimmune (rheumatoid) arthritis, multiple sclerosis, transplant rejection, Crohn's disease, ulcerative colitis, dermatitis, and the like. In some embodiments, the cells are chimeric autoantibody receptor T-cells, or CAAR-Ts displaying antigens or fragments thereof, instead of antibody fragments; in this version of adoptive cell transfer, the B cells that cause autoimmune diseases will attempt to attack the engineered T cells, which will respond by killing them.

In some embodiments, the cells may be used in the treatment of infectious diseases such as HIV and tuberculosis.

In another embodiment, the CAR-T cells of the present disclosure can undergo robust in vivo T cell expansion and can persist for an extended amount of time.

In some embodiments, the treatment of a patient with CAR-T cells of the present disclosure can be ameliorating, curative or prophylactic. It may be either part of an autologous immunotherapy or part of an allogenic immunotherapy treatment. By autologous, it is meant that cells, cell line or population of cells used for treating patients are originating from said patient or from a Human Leucocyte Antigen (HLA) compatible donor. By allogeneic, is meant that the cells or population of cells used for treating patients are not originating from the patient but from a donor.

The treatment of cancer with CAR-T cells of the present disclosure may be in combination with one or more therapies selected from antibody therapy, chemotherapy, cytokine therapy, dendritic cell therapy, gene therapy, hormone therapy, radiotherapy, laser light therapy, and radiation therapy.

The administration of CAR-T cells or a population of CAR-T cells of the present disclosure of the present disclosure be carried out by aerosol inhalation, injection, ingestion, transfusion, implantation or transplantation. The CAR-T cells compositions described herein, i.e., mono CAR, dual CAR, tandem CARs, may be administered to a patient subcutaneously, intradermally, intratumorally, intranodally, intramedullary, intramuscularly, by intravenous or intralymphatic injection, or intraperitoneally. In one embodiment, the cell compositions of the present disclosure are preferably administered by intravenous injection.

The administration of CAR-T cells or a population of CAR-T cells can consist of the administration of 10⁴-10⁹ cells per kg body weight, preferably 10⁵ to 10⁶ cells/kg body weight including all integer values of cell numbers within those ranges. The CAR-T cells or a population of CAR-T cells can be administrated in one or more doses. In another embodiment, the effective amount of CAR-T cells or a population of CAR-T cells are administrated as a single dose. In another embodiment, the effective amount of cells are administered as more than one dose over a period time. Timing of administration is within the judgment of a health care provider and depends on the clinical condition of the patient. The CAR-T cells or a population of CAR-T cells may be obtained from any source, such as a blood bank or a donor. While the needs of a patient vary, determination of optimal ranges of effective amounts of a given CAR-T cell population(s) for a particular disease or conditions are within the skill of the art. An effective amount means an amount which provides a therapeutic or prophylactic benefit. The dosage administered will be dependent upon the age, health and weight of the patient recipient, type of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.

In another embodiment, the effective amount of CAR-T cells or a population of CAR-T cells or composition comprising those CAR-T cells are administered parenterally. The administration can be an intravenous administration. The administration of CAR-T cells or a population of CAR-T cells or composition comprising those CAR-T cells can be directly done by injection within a tumor.

In one embodiment of the present disclosure, the CAR-T cells or a population of the CAR-T cells are administered to a patient in conjunction with, e.g., before, simultaneously or following, any number of relevant treatment modalities, including but not limited to, treatment with cytokines, or expression of cytokines from within the CAR-T, that enhance T-cell proliferation and persistence and, include but not limited to, IL-2, IL-7, and IL-15.

In a second embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with agents that inhibit immunosuppressive pathways, including but not limited to, inhibitors of TGF-β, interleukin 10 (IL-10), adenosine, VEGF, indoleamine 2,3 dioxygenase 1 (IDO1), indoleamine 2,3-dioxygenase 2 (IDO2), tryptophan 2-3-dioxygenase (TDO), lactate, hypoxia, arginase, and prostaglandin E2.

In another embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with T-cell checkpoint inhibitors, including but not limited to, anti-CTLA4 (Ipilimumab) anti-PD1 (Pembrolizumab, Nivolumab, Cemiplimab), anti-PDL1 (Atezolizumab, Avelumab, Durvalumab), anti-PDL2, anti-BTLA, anti-LAG3, anti-TIM3, anti-VISTA, anti-TIGIT, and anti-KIR.

In another embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with T cell agonists, including but not limited to, antibodies that stimulate CD28, ICOS, OX-40, CD27, 4-1BB, CD137, GITR, and HVEM

In another embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with therapeutic oncolytic viruses, including but not limited to, retroviruses, picornaviruses, rhabdoviruses, paramyxoviruses, reoviruses, parvoviruses, adenoviruses, herpesviruses, and poxviruses.

In another embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with immunostimulatory therapies, such as toll-like receptors agonists, including but not limited to, TLR3, TLR4, TLR7 and TLR9 agonists.

In another embodiment, the CAR-T cells or a population of CAR-T cells of the present disclosure may be used in combination with stimulator of interferon gene (STING) agonists, such as cyclic GMP-AMP synthase (cGAS).

Immune effector cell aplasia, particularly T cell aplasia is also a concern after adoptive cell transfer therapy. When the malignancy treated is a T-cell malignancy, and CAR-T cells target a T cell antigen, normal T cells and their precursors expressing the antigen will become depleted, and the immune system will be compromised. Accordingly, methods for managing these side effects are attendant to therapy. Such methods include selecting and retaining non-malignant T cells or precursors, either autologous or allogeneic (optionally engineered not to cause rejection or be rejected), for later expansion and re-infusion into the patient, after CAR-T cells are exhausted or deactivated. Alternatively, CAR-T cells which recognize and kill subsets of TCR-bearing cells, such as normal and malignant TRBC1⁺, but not TRBC2⁺ cells, or alternatively, TRBC2⁺, but not TRBC1⁺ cells, may be used to eradicate a T cell malignancy while preserving sufficient normal T cells to maintain normal immune system function.

Definitions

As used herein, the terms below have the meanings indicated. Other definitions may occur throughout the specification.

When ranges of values are disclosed, and the notation “from n₁ . . . to n₂” or “between n₁ . . . and n₂” is used, where n₁ and n₂ are the numbers, then unless otherwise specified, this notation is intended to include the numbers themselves and the range between them. This range may be integral or continuous between and including the end values. By way of example, the range “from 2 to 6 carbons” is intended to include two, three, four, five, and six carbons, since carbons come in integer units. Compare, by way of example, the range “from 1 to 3 μM (micromolar),” which is intended to include 1 μM, 3 μM, and everything in between to any number of significant figures (e.g., 1.255 μM, 2.1 μM, 2.9999 μM, etc.).

The term “about,” as used herein, is intended to qualify the numerical values which it modifies, denoting such a value as variable within a margin of error. When no particular margin of error, such as a standard deviation to a mean value given in a chart or table of data, is recited, the term “about” should be understood to mean that range which would encompass the recited value and the range which would be included by rounding up or down to that figure as well, taking into account significant figures.

The term “activation” (and other conjugations thereof) in reference to cells is generally understood to be synonymous with “stimulating” and as used herein refers to treatment of cells that results in expansion of cell populations. In T cells, activation is often accomplished by exposure to CD2 and CD28 (and sometimes CD2 as well) agonists, typically antibodies, optionally coated onto magnetic beads or conjugated to a colloidal polymeric matrix.

The term “antigen” as used herein is a cell surface protein recognized by (i.e., that is the target of) T cell receptor or chimeric antigen receptor. In the classical sense antigens are substances, typically proteins, that are recognized by antibodies, but the definitions overlap insofar as the CAR comprises antibody-derived domains such as light (V_(L)) and heavy (V_(H)) chains recognizing one or more antigen(s).

The term “cancer” refers to a malignancy or abnormal growth of cells in the body. Many different cancers can be characterized or identified by particular cell surface proteins or molecules. Thus, in general terms, cancer in accordance with the present disclosure may refer to any malignancy that may be treated with an immune effector cell, such as a CAR-T cell as described herein, in which the immune effector cell recognizes and binds to the cell surface protein on the cancer cell. As used herein, cancer may refer to a hematologic malignancy, such as multiple myeloma, a T-cell malignancy, or a B cell malignancy. T cell malignancies may include, but are not limited to, T-cell acute lymphoblastic leukemia (T-ALL) or non-Hodgkin's lymphoma. A cancer may also refer to a solid tumor, such as including, but not limited to, cervical cancer, pancreatic cancer, ovarian cancer, mesothelioma, and lung cancer.

A “cell surface protein” as used herein is a protein (or protein complex) expressed by a cell at least in part on the surface of the cell. Examples of cell surface proteins include the TCR (and subunits thereof) and CD7.

The term “combination therapy” means the administration of two or more therapeutic agents to treat a therapeutic condition or disorder described in the present disclosure. Such administration encompasses co-administration of these therapeutic agents in a substantially simultaneous manner, such as in a single capsule having a fixed ratio of active ingredients or in multiple, separate capsules for each active ingredient. In addition, such administration also encompasses use of each type of therapeutic agent in a sequential manner. In either case, the treatment regimen will provide beneficial effects of the drug combination in treating the conditions or disorders described herein.

The term “composition” as used herein refers to an immunotherapeutic cell population combination with one or more therapeutically acceptable carriers.

The term “disease” as used herein is intended to be generally synonymous, and is used interchangeably with, the terms “disorder,” “syndrome,” and “condition” (as in medical condition), in that all reflect an abnormal condition of the human or animal body or of one of its parts that impairs normal functioning, is typically manifested by distinguishing signs and symptoms, and causes the human or animal to have a reduced duration or quality of life.

The term “donor template” refers to the reference genomic material that the cell uses as a template to repair the a double-stranded break through the homology-directed repair (HDR) DNA repair pathway. The donor template contains the piece of DNA to be inserted into the genome (containing the gene to be expressed, CAR, or marker) with two homology arms flanking the site of the double-stranded break. In some embodiments, a donor template may be an adeno-associated virus, a single-stranded DNA, or a double-stranded DNA.

The term “fratricide” as used herein means a process which occurs when a CAR-T cell (or other CAR-bearing immune effector cell) becomes the target of, and is killed by, another CAR-T cell comprising the same chimeric antigen receptor as the target of CAR-T cell, because the targeted cell expresses the antigen specifically recognized by the chimeric antigen receptor on both cells. CAR-T comprising a chimeric antigen receptor which are deficient in an antigen to which the chimeric antigen receptor specifically binds will be “fratricide-resistant.”

The term “genome-edited” or “gene-edited” as used herein means having a gene or portion of the genome added, deleted, or modified (e.g., disrupted) to be non-functional. Thus, in certain embodiments, a “genome-edited T cell” is a T cell that has had a gene such as a CAR recognizing at least one antigen added; and/or has had a gene such as the gene(s) to the antigen(s) that are recognized by the CAR deleted, and/or has had the gene to the TCR or a subunit thereof disrupted.

A “healthy donor,” as used herein, is one who does not have a malignancy (particularly a hematologic malignancy, e.g., a T-cell malignancy).

As used herein, an “immature dendritic cell” or “iDC” refers to an immature dendritic cell.

The term “therapeutically acceptable” refers to substances which are suitable for use in contact with the tissues of patients without undue toxicity, irritation, and allergic response, are commensurate with a reasonable benefit/risk ratio, and/or are effective for their intended use.

The term “therapeutically effective” is intended to qualify the amount of active ingredients used in the treatment of a disease or disorder or on the effecting of a clinical endpoint.

The term “patient” is generally synonymous with the term “subject” and includes all mammals including humans.

A “malignant B cell” is a B cell derived from a B-cell malignancy. B cell malignancies include, without limitation, (DLBCL), chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL), and B cell-precursor acute lymphoblastic leukemia (ALL).

The term “exposing to,” as used herein, in the context of bringing compositions of matter (such as antibodies) into intimate contact with other compositions of matter (such as cells), is intended to be synonymous with “incubated with,” and no lengthier period of time in contact is intended by the use of one term instead of the other.

A “malignant T cell” is a T cell derived from a T-cell malignancy. The term “T-cell malignancy” refers to a broad, highly heterogeneous grouping of malignancies derived from T-cell precursors, mature T cells, or natural killer cells. Non-limiting examples of T-cell malignancies include T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), human T-cell leukemia virus type 1-positive (HTLV-1+) adult T-cell leukemia/lymphoma (ATL), T-cell prolymphocytic leukemia (T-PLL), Adult T-cell lymphoma/leukemia (HTLV-1 associated), Aggressive NK-cell leukemia, Anaplastic large-cell lymphoma (ALCL), ALK positive, Anaplastic large-cell lymphoma (ALCL), ALK negative, Angioimmunoblastic T-cell lymphoma (AITL), Breast implant-associated anaplastic large-cell lymphoma, Chronic lymphoproliferative disorder of NK cells, Extra nodal NK/T-cell lymphoma, nasal type, Enteropathy-type T-cell lymphoma, Follicular T-cell lymphoma, Hepatosplenic T-cell lymphoma, Indolent T-cell lymphoproliferative disorder of the GI tract, Monomorphic epitheliotrophic intestinal T-cell lymphoma, Mycosis fungoides, Nodal peripheral T-cell lymphoma with TFH phenotype, Peripheral T-cell lymphoma (PTCL), NOS, Primary cutaneous a/p T-cell lymphoma, Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma, Primary cutaneous acral CD8+ T-cell lymphoma, Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorders [Primary cutaneous anaplastic large-cell lymphoma (C-ALCL), lymphoid papulosis], Sezary syndrome, Subcutaneous, panniculitis-like T-cell lymphoma, Systemic EBV+ T-cell lymphoma of childhood, and T-cell large granular lymphocytic leukemia (LGL).

A “malignant plasma cell” is a plasma cell derived from a plasma cell malignancy. The term “plasma-cell malignancy” refers to a malignancy in which abnormal plasma cells are overproduced. Non-limiting examples of plasma cell malignancies include lymphoplasmacytic lymphoma, plasmacytoma, and multiple myeloma.

As used herein, “suicide gene” refers to a nucleic acid sequence introduced to a CAR-T cell by standard methods known in the art, that when activated result in the death of the CAR-T cell. If required suicide genes may facilitate the tracking and elimination, i.e., killing, of CAR-T cells in vivo. Facilitated killing of CAR-T cells by activating a suicide gene can be accomplished by standard methods known in the art. Suicide gene systems known in the art include, but are not limited to, several herpes simplex virus thymidine kinase (HSVtk)/ganciclovir (GCV) suicide gene therapy systems and inducible caspase 9 proteins. In one embodiment, the suicide gene is a chimeric CD34/thymidine kinase.

As used herein, an “immune effector cell” is a leukocyte that can modulate an immune response. Immune effector cells include T cells, B cells, natural killer (NK) cells, iNKT cells (invariant T-cell receptor alpha natural killer T cells), and macrophages. T cell receptor (TCR)-bearing immune effector cells include, of course, T cells, but also cells which have been engineered to express a T cell receptor. Immune effector cells may be obtained or derived/generated from any appropriate source, such as including, but not limited to, healthy donors, peripheral blood mononuclear cells, cord blood, and induced pluripotent stem cells (iPSC).

As used herein, a “CAR-bearing immune effector cell” is an immune effector cell which has been transduced with at least one CAR. A “CAR-T cell” is a T cell which has been transduced with at least one CAR; CAR-T cells can be mono, dual, or tandem CAR-T cells. CAR-T cells can be autologous, meaning that they are engineered from a subject's own cells, or allogeneic, meaning that the cells are sourced from a healthy donor, and in many cases, engineered so as not to provoke a host-vs-graft or graft-vs-host reaction.

A “chimeric antigen receptor” or “CAR” as used herein and generally used in the art, refers to a recombinant fusion protein that has an extracellular ligand-binding domain, a transmembrane domain, and a signaling transducing domain that directs the cell to perform a specialized function upon binding of the extracellular ligand-binding domain to a component present on the target cell. For example, a CAR can have an antibody-based specificity for a desired antigen (e.g., tumor antigen) with a T cell receptor-activating intracellular domain to generate a chimeric protein that exhibits specific anti-target cellular immune activity. First-generation CARs include an extracellular ligand-binding domain and signaling transducing domain, commonly CD3ζ or FcεRIγ. Second generation CARs are built upon first generation CAR constructs by including an intracellular costimulatory domain, commonly 4-1BB or CD28. These costimulatory domains help enhance CAR-T cell cytotoxicity and proliferation compared to first generation CARs. The third generation CARs include multiple costimulatory domains, primarily to increase CAR-T cell proliferation and persistence. Chimeric antigen receptors are distinguished from other antigen binding agents by their ability both to bind MHC-independent antigens and transduce activation signals via their intracellular domain.

The term “CAR-iNKT cell” (equivalently, iNKT-CAR) means an iNKT cell that expresses a chimeric antigen receptor. A dual iNKT-CAR cell (equivalently, iNKT-dCAR) is an iNKT-CAR cell that expresses two distinct chimeric antigen receptor polypeptides with affinity to different target antigens expressed within the same effector cell, wherein each CAR functions independently. The CAR may be expressed from a single or multiple polynucleotide sequences. A tandem iNKT-CAR cell (equivalently, iNKT-tCAR) is an iNKT-CAR cell with a single chimeric antigen polypeptide containing two distinct antigen recognition domains with affinity to different targets, wherein the antigen recognition domains are linked through a peptide linker and share common costimulatory domain(s), and wherein binding of either antigen recognition domain will signal though a common costimulatory domains(s) and signaling domain.

The term “chimeric antigen receptor T cell” (equivalently, CAR-T) means an T cell that expresses a chimeric antigen receptor.

The term dual CAR-T (dCAR-T), means a CAR-T cell that expresses cells two distinct chimeric antigen receptor polypeptides with affinity to different target antigen expressed within the same effector cell, wherein each CAR functions independently. The CAR may be expressed from single or multiple polynucleotide sequences.

The term tandem CAR-T (tCAR-T) means a single chimeric antigen polypeptide containing two distinct antigen recognition domains with affinity to different targets wherein the antigen recognition domain is linked through a peptide linker and share common costimulatory domain(s), wherein the binding of either antigen recognition domain will signal through a common co-stimulatory domains(s) and signaling domain.

As used herein, a chimeric antigen receptor natural killer (NK) cell (equivalently, NK-CAR) would have a meaning analogous to the definitions of CAR-T and iNKT-CAR.

As used herein, a chimeric antigen receptor macrophage (equivalently, CAR-macrophage) would have a meaning analogous to the definitions of CAR-T, iNKT-CAR, and NK-CAR.

As used herein, the term “cytokine release syndrome” refers to a condition that may occur after treatment with some types of immunotherapy, such as monoclonal antibodies and CAR-T or other CAR-bearing immune effector cells. Cytokine release syndrome is caused by a large, rapid release of cytokines into the blood from immune cells affected by the immunotherapy. Symptoms of CRS include fever, fatigue, loss of appetite, muscle and joint pain, nausea, vomiting, diarrhea, rashes, fast breathing, rapid heartbeat, low blood pressure, seizures, headache, confusion, delirium, hallucinations, tremor, and loss of coordination. CRS can manifest along a spectrum of mild to fatal, and can be ranked by severity as follows:

-   -   Grade 1: Mild reaction, infusion interruption not indicated;         intervention not indicated     -   Grade 2: Therapy or infusion interruption indicated but responds         promptly to symptomatic treatment (e.g., antihistamines, NSAIDS,         narcotics, IV fluids); prophylactic medications indicated for         <=24 hrs     -   Grade 3: Prolonged (e.g., not rapidly responsive to symptomatic         medication and/or brief interruption of infusion); recurrence of         symptoms following initial improvement; hospitalization         indicated for clinical sequelae (e.g., renal impairment,         pulmonary infiltrates)     -   Grade 4: Life-threatening consequences; pressor or ventilatory         support indicated     -   Grade 5: Death         See, e.g., “Common Terminology Criteria for Adverse Events         (CTCAE) Version v4.03,” National Institutes of Health and         National Cancer Institute, Jun. 14, 2010; Lee D W et al.,         “Current concepts in the diagnosis and management of cytokine         release syndrome,” Blood 2014 124(2):188-95.

As used herein, the term “CAR-T associated neuropathy” means neuropathy that arises subsequent to administration of CAR-T therapy to a patient, often after intervening cytokine release syndrome has occurred and subsided. The term is relatively new, mainly because CAR-T therapy is relatively new; see, e.g., Vasthie P and Breitbart W S, “Chimeric antigen receptor T-cell neuropsychiatric toxicity in acute lymphoblastic leukemia,” Palliat Support Care. 2017 August; 15(4): 499-503. Accordingly, CAR-T associated neuropathy should be understood at this time to be equivalent to the term “CAR-bearing immune effector cell associated neuropathy,” since similar neuropathy could arise from therapy with, e.g., iNKT-CARs or NK-CARs.

As used herein, a “cytokine” is one of a class of small (˜5-20 kDa), soluble signaling proteins that are that are synthesized and secreted by certain cells of the immune system at variable, and occasionally locally high, concentrations and by binding to receptors on other cells, send signals to and have an effect on those cells. A “chemokine” is a chemotactic cytokine, i.e., a subspecies of cytokine that is able to induce chemotaxis in nearby responsive cells.

As used herein, to be “deficient” in a cytokine or protein means to lack sufficient quantity of the cytokine or protein for the cytokine or protein to elicit its normal effect. A cell that is “deficient” in GM-CSF, for example, (a “GM-CSF deficient” cell) could be entirely lacking in GM-CSF, but it also could express such a negligible quantity of GM-CSF that the GM-CSF present could not contribute in any meaningful way to the development or maintenance of cytokine release syndrome.

The term “deletion” as used herein in reference to the effect of editing on a gene or its protein product, means alteration or loss of part the sequence of DNA encoding the protein so as to reduce or prevent expression of the protein product. The term “suppression” in the same context means to reduce expression of the protein product; and the term “ablation” in the same context means to knock out (KO) or prevent expression of the protein product. Deletion encompasses suppression and ablation.

As used herein, a “secretable protein” is s protein secreted by a cell which has an effect on other cells. By way of example, secretable proteins include cytokines, chemokines, and transcription factors.

As used herein, a “selectable marker” refers to a marker that allows distinguishing between different cell types, such as a cell into which a CAR has been successfully inserted (i.e., a gene-edited or modified cell). Selectable markers are well known in the art and materials and methods for their use are readily available. In some embodiments, a selectable marker appropriate in accordance with the present disclosure may be a fluorescent protein gene, such as including, but not limited to, a green fluorescence (GFP) gene or a yellow fluorescent protein (YFP) gene. In some embodiments, a selectable marker may be a splice variant of a CD34 gene, such as a truncated CD34 (tCD34) gene or a truncated EGFR (tEGFR) gene. In some embodiments, a selectable marker described herein, such as GFP, or others known and available in the art, may be inserted alone into a gene as described herein (i.e., without a CAR), or may be inserted as a component of a construct comprising the selectable marker and a CAR.

As used herein, a “short hairpin RNA” or “small hairpin RNA” (shRNA) is an artificial RNA molecule, often about 80 base pairs in length and with a tight hairpin turn, that can be used to silence target gene expression via processing within the cell into siRNA which in turn knocks down gene expression. ShRNAs can be incorporated into genomic DNA, and provide stable and long-lasting expression.

As used herein, “transduction” is the process by which foreign DNA is introduced into a cell by a virus or viral vector such as a plasmid, for example by short hairpin RNAs (shRNAs); it often provides long-lasting or permanent silencing of a gene. It may be accomplished by methods known in the art, including electroporation.

Transfection is the process of deliberately introducing purified nucleic acids into eukaryotic cells, for example small interfering RNAs (siRNAs); it produces transient silencing of a gene by RNA interference with mRNA transcripts. Transduction is the process by which foreign DNA is introduced into a cell by a virus or viral vector such as a plasmid, for example by short hairpin RNAs (shRNAs); it often provides long-lasting or permanent silencing of a gene. Both may be accomplished by methods known in the art, including electroporation.

EXAMPLES

The invention is further illustrated by the following examples.

Example 1—Method of Blocking Gene Translation by CAR Insertion

FIG. 1 shows the deletion of a cytokine gene by using Cas9/CRISPR to target a locus in a cytokine gene, then use homology-directed repair to insert the CAS construct. Optionally, the CAS construct would contain a marker, such as a selectable marker as described herein. One challenge with this concept is that is hard to select and sort out the cells have been edited from those that still express the cytokine/chemokine. One way to overcome this is to insert the CAR construct containing a marker, into gene that has been deleted. It has previously been demonstrated that inserting CAR19 into the TRAC gene allows the selection of TRAC-negative, CAR-positive cells. This would allow sorting of cells that have both expression of the car and have the cytokine deleted. Another alternative would be to express a shRNA from the CAR construct that would degrade the RNA encoding for the cytokine without altering the genome. A marker on the CAR construct (such as the truncated CD34 marker) could be used to select cells that downregulate the cytokine and express the CAR, i.e., CAR+=Cytokine negative.

As shown in FIG. 2 , CAR-bearing immune effector cells (e.g., CAR-T) would be activated for two days prior to gene editing to delete the target cytokine gene and transduction of CAR.

Example 2—General Method of Making Genome-Edited CAR-Bearing Immune Effector Cells

Further details regarding the manner of making CAR-bearing immune effector cells are known in the art, e.g., as disclosed in WO2018027036A1.

The following general steps may be taken to provide CAR-bearing immune effector cells. As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Step 1. Cells are harvested, isolated, and purified, for example using magnetic selection with a labelled antibody-coated magnetic beads that bind to a cell-specific protein (available from, e.g., Miltenyi Biotec). For T cells, anti-CD3/CD28 beads could be used. Other purification techniques are known in the art and could be used.

Step 3. Cells are thereafter activated. There are several ways to activate immune effector cells. For example, T cells may be activated using antiCD3/CD28 beads for two days prior to bead removal. Alternatively, an antibody could be used.

Step 4. The antigen that is the target of the CAR may be deleted from the cell surface or its expression suppressed to prevent subsequent fratricide. Target deletion may be accomplished by electroporation with Cas9 mRNA and gRNA against the target(s). Other techniques, however, could be used to suppress expression of the target. These include other genome editing techniques such as TALENs, ZFNs, RNA interference, and eliciting of internal binding of the antigen to prevent cell surface expression. Deletion of the target may not be required in every circumstance. Examples of gRNAs that may be used include those shown in Tables 8-10, as well as others known in the art.

TABLE 8 Guide RNA sequences for use in removing surface antigens on immune effector cells Target gene gRNA sequence CD7 5′_2′OMe(A(ps)U(pS)C(ps))ACGGAGGUCAAUGUCUAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ (SEQ ID NO: 40) CD7g10 5′_2′OMe(G(ps)U(ps)A(ps))GACAUUGACCUCCGUGAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ (SEQ ID NO: 41) CD7g4 5′_2′OMe(A(ps)U(ps)C(ps))ACGGAGGUCAAUGUCUAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U _3′ (SEQ ID NO: 42) TRACg 5′_2′OMe(G(ps)A(ps)G(ps))AAUCAAAAUCGGUGAAUGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ (SEQ ID NO: 43) CS1 5′_2′OMe(G(ps)A(ps)C(ps))CAAUCUGACAUGCUGCAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ (SEQ ID NO: 44) CD2 5′_2′OMe(A(ps)C(ps)A(ps))GCUGACAGGCUCGACACGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps) U_3′ (SEQ ID NO: 45) CD2g 5′_2′OMe(G(ps)A(ps)G(ps))AAUCAAAAUCGGUGAAUGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps) U 3′ (SEQ ID NO: 46) CD3ϵg 5′_2′OMe(A(ps)G(ps)G(ps))GCAUGUCAAUAUUACUGGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps) U 3′ (SEQ ID NO: 47) CD5 5′_2′OMe(C(ps)G(ps)U(ps))UCCAACUCGAAGUGCCAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps))U3′ (SEQ ID NO: 48) CD5g 5′_2′OMe(C(ps)G(ps)U(ps))uCCAACUCGAAGUGCCAGUUUUAGAGCUAGA AAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUG GCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ (SEQ ID NO: 49) RNA; (ps) indicate phosphorothioate. Underlined bases denote target sequence.

Step 5. Cells may then be transduced with a CAR targeted to (i.e., that recognizes) one or more antigen or protein targets, for example with a lentivirus containing a CAR construct. Any other suitable method of transduction/transfection may be used, for example transfection using DNA-integrating viral or non-viral vectors containing transposable elements, or transient expressing of non-DNA integrating polynucleotides, such as mRNA, or insertion of CAR polynucleotide into site of nuclease activity using homologous or non-homologous recombination.

Step 6. CAR-bearing immune effector cells are then cultured to expand their population.

Example 3—Method of Making Genome-Edited Tandem CAR-Bearing Immune Effector Cells

In a variation of the protocol in the example above, a tCAR cell recognizing two antigens can be made. In Step 4, the two antigens can be deleted from the cell surface, or suppressed as described above, but electroporation with gRNA for each of the two targets and Cas9 mRNA. In Step 5, cells are then transduced with a CAR that recognizes two targets.

Example 4—Method of Making Genome-Edited Dual CAR-Bearing Immune Effector Cells

In a variation of the protocol in the example above, a dCAR cell targeting two antigens can be made. This variation would contain two separate CARs, each recognizing a different antigen.

Example 5—Method of Making and Testing a Genome-Edited CAR-T Cell with Suppressed Expression of Cytokine or Chemokine

The following steps may be taken to provide a genome-edited CAR-T cell with suppressed expression and/or secretion of a specific cytokine or chemokine. This example describes the making of a CD19 targeting CAR-T which is deficient in expression of GM-CSF. As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Tumor is injected into SCID-Beige mice (3e6 Raji containing Luciferase) if performing in vivo CRS experiment. This should be completed 3 weeks prior to infusion of CAR-T into mice.

T Cell Activation (Day 0).

T cells are purified via leukapheresis chamber using a Miltenyi human PanT isolation kit, then resuspended in media. Cells are counted and the number of human T cell activation CD3/CD28 beads required to obtain 3:1 bead:cell ratio determined. Beads are washed 2× with T cell media, then cells diluted at 1.256 cells/mL in hXcyte media. Human T cell activation CD3/CD28 beads are added. Into each well of a 6-well plate are aliquoted 4 mL/well of 1.256 cell/mL solution. Cells are incubated at 37° C.

CRISPR (Day 2).

Target deletion may be accomplished by electroporating with Cas9 mRNA and gRNA against the target(s). Other techniques, however, could be used to suppress expression of the target. These include other genome editing techniques such as TALENs, RNA interference, and eliciting of internal binding of the antigen to prevent cell surface expression. Examples of gRNAs that may be used include those shown in Tables 8-10, as well as others known in the art.

Nucleofection Sample ID gRNA#1 Cas9 Buffer P3 20 μg gGM-CSF 15 μg Cas9 mRNA 100 μl

TABLE 9 Guide RNA sequences for use in reducing CRS Target gene gRNA sequence GM-CSF 5′_2′OMe(U(ps)A(ps)C(ps))UCAGGUU CAGGAGACGCGUUUUAGAGCUAGAAAUAGCAA GUUAAAAUAAGGCUAGUCCGUUAUCAACUUGA AAAAGUGGCACCGAGUCGGUGC 2′OMe (U(ps)U(ps)U(ps)U _3′ (SEQ ID NO: 50) RNA; (ps) indicate phosphorothioate. Underlined bases denote target sequence.

TABLE 10 Additional guide RNA sequences for use in reducing the incidence of CRS Target Gene SEQ ID Symbol Guide RNA Sequence NO:  Location Gene ID No. A2M GACAAAUCAAUCUACAAACC 56 chr12 ENST00000318602.11 A2M GGUCCGCUUCUUAAAUUCUU 57 chr12 ENST00000318602.11 A2M UCCUCAUUGGAUGAAGACUU 58 chr12 ENST00000318602.1 ACKR1 AACUGAGAACUCAAGUCAGC 59 chr1 ENST00000368122.2 ACKR1 GAAGGAAUCAUUCACACCAU 60 chr1 ENST00000368122.2 ACKR1 ACACUGGUGAGGAUGAAGAA 61 chr1 ENST00000368122.2 ACKR2 UCGGCAUCCUCAGUGGCGAG 62 chr3 ENST00000422265.5 ACKR2 GCAUGAAGGCCACUUCAUCC 63 chr3 ENST00000422265.5 ACKR2 AAAUCAGGCUAUAGAAGACU 64 chr3 ENST00000422265.5 ACKR3 UAGAGCAGGACGCUUUUGUU 65 chr2 ENST00000272928.3 ACKR3 CGGCAUGAUUGCCAACUCCG 66 chr2 ENST00000272928.3 ACKR3 CCCACAGGUCGGCAAUGGCC 67 chr2 ENST00000272928.3 ACVR1 UCUUUCCCUGCUCAUAAACC 68 chr2 ENST00000263640.7 ACVR1 UCCUCACUGAGCAUCAACGA 69 chr2 ENST00000263640.7 ACVR1 CUCUACAUGUGUGUGUGUGA 70 chr2 ENST00000263640.7 ACVR2B CUACAACGCCAACUGGGAGC 71 chr3 ENST00000352511.4 ACVR2B GCCAGAGCUGUUGCGCCAGG 72 chr3 ENST00000352511.4 ACVR2B AUGACUUCAACUGCUACGAU 73 chr3 ENST00000352511.4 ACVRL1 AGACCCUGUGAAGCCGUCUC 74 chr12 ENST00000388922.8 ACVRL1 GGCCUACCUGCCGGGGGGCC 75 chr12 ENST00000388922.8 ACVRL1 GGGGCUGCGGGAACUUGCAC 76 chr12 ENST00000388922.8 ADIPOQ GGGCUCAGGAUGCUGUUGCU 77 chr3 ENST00000320741.6 ADIPOQ CGUGGUUUCCUGGUCAUGAC 78 chr3 ENST00000320741.6 ADIPOQ GGGGGCCUGCACAGGUUGGA 79 chr3 ENST00000320741.6 AGER ACGGACUCGGUAGUUGGACU 80 chr6 ENST00000375076.8 AGER CUGUCGGGAUCCAGGAUGAG 81 chr6 ENST00000375076.8 AGER UCCCCAGGGAGGAGGCCCCU 82 chr6 ENST00000375076.8 AGRN CGGGGAAUGCUGUGCGGCUU 83 chr1 ENST00000379370.6 AGRN GAAGAGCCCGUGCCCCAGCG 84 chr1 ENST00000379370.6 AGRN GCAUUCGUUGCUGUAGGUGG 85 chr1 ENST00000379370.6 AHR UUGAUUCCUUCAGCUGGGAU 86 chr7 ENST00000242057.8 AHR GUAAAGCCAAUCCCAGCUGA 87 chr7 ENST00000242057.8 AHR UUGACUUGAUUCCUUCAGCU 88 chr7 ENST00000242057.8 AHR UUUGACUUGAUUCCUUCAGC 89 chr7 ENST00000242057.8 AIMP1 AACCAAUUCGAAGAUCCAGA 90 chr4 ENST00000358008.7 AIMP1 UAUGUGGAAGAAGUAGAUGU 91 chr4 ENST00000358008.7 AIMP1 CAAGAGGAACAUGAUUCACC 92 chr4 ENST00000358008.7 AREG GGUCCAAUCCAGCAGCAUAA 93 chr4 ENST00000395748.7 AREG CCACAGUGCUGAUGGAUUUG 94 chr4 ENST00000395748.7 AREG AGAAGGCAUUUCACUCACAG 95 chr4 ENST00000395748.7 BCL6 CUGUAAAGAUGCUAUAGAAC 96 chr3 ENST00000406870.6 BCL6 CACUAAGGUUGCAUUUCAAC 97 chr3 ENST00000406870.6 BCL6 GAUCUAGAUUGAUCACACUA 98 chr3 ENST00000406870.6 BCL6 AAUCCCUCAGGGUUGAUCUC 99 chr3 ENST00000406870.6 BMP1 CAGCGGCAGGCGGGCCACGC 100 chr8 ENST00000306385.9 BMP1 GGCCGACUACACCUAUGACC 101 chr8 ENST00000306385.9 BMP1 GGCGCUCACCCGCCUUGCAG 102 chr8 ENST00000306385.9 BMP10 GAAACUCAUCCUUCAUGCUC 103 chr2 ENST00000295379.1 BMP10 AGGGACAUAUCUUCUUCCAG 104 chr2 ENST00000295379.1 BMP10 CAGAAACCAAGUAAGCUGCC 105 chr2 ENST00000295379.1 BMP15 CGUGCUUUUCAUGGAACACA 106 chrX ENST00000252677.3 BMP15 CCCUACUUUGCCCCUGAUUG 107 chrX ENST00000252677.3 BMP15 AGUGAAUGCCCUAGGAGCCG 108 chrX ENST00000252677.3 BMP2 CGCAGGUCGACCAUGGUGGC 109 chr20 ENST00000378827.4 BMP2 GGGCCGCAGGAAGUUCGCGG 110 chr20 ENST00000378827.4 BMP2 GCCGCAACUCGAACUCGCUC 111 chr20 ENST00000378827.4 BMP3 AGGCUGCUCUUUCUGUGGCU 112 chr4 ENST00000282701.2 BMP3 GGCACAGCUUUGCGGAGCUC 113 chr4 ENST00000282701.2 BMP3 CGAGCUGCAGCCGCAAGACA 114 chr4 ENST00000282701.2 BMP4 UUCGUGGUGGAAGCUCCUCA 115 chr14 ENST00000245451.8 BMP4 GAAGAGCAGAUCCACAGCAC 116 chr14 ENST00000245451.8 BMP4 CACUCUUGCUAGGCUGCGGG 117 chr14 ENST00000245451.8 BMP5 ACUGAGUACUCCGACUCUUC 118 chr6 ENST00000370830.3 BMP5 AGACCCAGACCAUUUUCACC 119 chr6 ENST00000370830.3 BMP5 CGAAAGACGGGAAAUACAAA 120 chr6 ENST00000370830.3 BMP6 GAUGCAGAAGGAGAUCUUGU 121 chr6 ENST00000283147.6 BMP6 GGCUGUUGGAGGCCGUGCAG 122 chr6 ENST00000283147.6 BMP6 CCUCGCGGAGAGCCCCCUCC 123 chr6 ENST00000283147.6 BMP7 UCUCAUUGUCGAAGCGUUCC 124 chr20 ENST00000395863.7 BMP7 GCCGUGACAGCUUCCCCUUC 125 chr20 ENST00000395863.7 BMP7 UCUUCCAGUGGAACAUGACA 126 chr20 ENST00000395863.7 BMP8A CCAGAAGCCAGAGCGGUCCG 127 chr1 ENST00000331593.5 BMP8A UGGCGGUGCUCGGGCUACCC 128 chr1 ENST00000331593.5 BMP8A UGGCGGUGCUCGGGCUACCC 129 chr1 ENST00000331593.5 BMP8B CGGUGCUCGGGCUGCCUGGG 130 chr1 ENST00000372827.7 BMP8B CCCAGGAGCCAGAGCGGGCC 131 chr1 ENST00000372827.7 BMP8B CCCAGGAGCCAGAGCGGGCC 132 chr1 ENST00000372827.7 BMPR2 CACUUGCAGCUGAUUGGCCG 133 chr2 ENST00000374580.8 BMPR2 UUUCGUUGAUAAAAUUCUGA 134 chr2 ENST00000374580.8 BMPR2 CUCAUCUCCAACUAUAAAGC 135 chr2 ENST00000374580.8 C10orf99 GGAAAGGACUAGAAGCCUCA 136 chr10 ENST00000372126.3 C10orf99 CCUACCUUCUGUGGAGAAGA 137 chr10 ENST00000372126.3 C10orf99 CUCUGAUCAGGAUUUGUUGG 138 chr10 ENST00000372126.3 C1QTNF4 CCAUCUCCGACGUGCCCUCC 139 chr11 ENST00000302514.3 C1QTNF4 CAGCUCAGAGGAUCCCGGGC 140 chr11 ENST00000302514.3 C1QTNF4 CCCAGCAGGCCCAGCAGAAG 141 chr11 ENST00000302514.3 C5* UCCAGCACCGUCACUCCAGA 142 chr9 ENST00000223642.2 C5* ACACGUGUUACACUUUUGCU 143 chr9 ENST00000223642.2 C5* GAUUCGCUUGACCAGUUGGU 144 chr9 ENST00000223642.2 CCL1* AGAAACGUGGUCAGCCACUC 145 chr17 ENST00000225842.3 CCL1* CUCUUGCUGUCCACAUCUUC 146 chr17 ENST00000225842.3 CCL1* GCAGAUCAUCACCACAGCCC 147 chr17 ENST00000225842.3 CCL11 AGGUCUCCGCAGCACUUCUG 148 chr17 ENST00000305869.3 CCL11 CUGGCCCAGCGAGCCCCUGG 149 chr17 ENST00000305869.3 CCL11 UAACCACCUCCAGAGCUACU 150 chr17 ENST00000305869.3 CCL13* AUGUGAAGCAGCAAGUAGAU 151 chr17 ENST00000225844.6 CCL13* CUUCUGGGGACACCUGCUGG 152 chr17 ENST00000225844.6 CCL13* AACUUUGGAUUGGGGAAUGU 153 chr17 ENST00000225844.6 CCL14 CAGGAGUGAGGUUGGGGCUC 154 chr17 ENST00000618404.4 CCL14 GGCAUUGCACUCACGUGAGG 155 chr17 ENST00000618404.4 CCL14 CCACAGCAUGAAGAUCUCCG 156 chr17 ENST00000618404.4 CCL15* UCCCAGAGCUUGAGUUACCA 157 chr17 ENST00000617897.1 CCL15* CACCAUUUGUGAACUGGGCC 158 chr17 ENST00000617897.1 CCL15* CACCAUUUGUGAACUGGGCC 159 chr17 ENST00000617897.1 CCL16 GGACGUGCUUACAUGAUUGC 160 chr17 ENST00000611905.1 CCL16 GUUGCCAAGGAGACUAGUGG 161 chr17 ENST00000611905.1 CCL16 UCCUUCAGAAGUUCCUGAGU 162 chr17 ENST00000611905.1 CCL17 GCUCCUCUCCCUGCAGCUCG 163 chr16 ENST00000219244.8 CCL17 UGGCUCCCUUGAAGUACUCC 164 chr16 ENST00000219244.8 CCL17 UGGAGCAGUCCUCAGAUGUC 165 chr16 ENST00000219244.8 CCL18 GAGGCAGCAGAGCUCUUUGU 166 chr17 ENST00000616054.1 CCL18 UGGCUUGGGGCACUGGGGGC 167 chr17 ENST00000616054.1 CCL18 CCAUCCUCCCUCCCGAGGGG 168 chr17 ENST00000616054.1 CCL19 CCCACAACUCACACUACAGC 169 chr9 ENST00000311925.6 CCL19 AAGUUCCUCACGAUGUACCC 170 chr9 ENST00000311925.6 CCL19 CAUUGGUGCCACUCAGAGUU 171 chr9 ENST00000311925.6 CCL2 GUUAUAACAGCAGGUGACUG 172 chr17 ENST00000225831.4 CCL2 UUCUUUGGGACACUUGCUGC 173 chr17 ENST00000225831.4 CCL2 GGCUUGUCCCUUGCUCCACA 174 chr17 ENST00000225831.4 CCL20 CAAACUCUUGGUACAGCACA 175 chr2 ENST00000358813.4 CCL20 CACCUCUGCGGCGAAUCAGA 176 chr2 ENST00000358813.4 CCL20 CAGUUGAGCUCAAGGCUAAA 177 chr2 ENST00000358813.4 CCL21 CCCUGCAGGCAGUGAUGGAG 178 chr9 ENST00000259607.6 CCL21 CCUCCCUGCCUUGGUACCUU 179 chr9 ENST00000259607.6 CCL21 GGCUCUGAGCCUCCUUAUCC 180 chr9 ENST00000259607.6 CCL22 ACCCCUCCCCUAGGCCCCUA 181 chr16 ENST00000219235.4 CCL22 GACGGUAACGGACGUAAUCA 182 chr16 ENST00000219235.4 CCL22 AGGCCUCGGGCAGGAGUCUG 183 chr16 ENST00000219235.4 CCL23* UCGUUUCAAAGUAACUCUCC 184 chr17 ENST00000615050.1 CCL23* AGCAGUCAGCACUAGUAGCA 185 chr17 ENST00000615050.1 CCL23* GUGCUCUGGAGGAGAAAGAU 186 chr17 ENST00000615050.1 CCL24 CCUCAAGGCAGGAGUGAUGU 187 chr7 ENST00000222902.6 CCL24 GAGAAUUCCUGAGAACCGAG 188 chr7 ENST00000222902.6 CCL24 CUCUCCUCUUCUAGGCUCUG 189 chr7 ENST00000222902.6 CCL25 UGUGGUUGCAGGUGUCUUUG 190 chr19 ENST00000390669.7 CCL25 GGGCUGUGCUCCGGCGCGCC 191 chr19 ENST00000390669.7 CCL25 GGCCCCACUCACAUCGCAGC 192 chr19 ENST00000390669.7 CCL26 CCAUCCUGUUGCAUGACUGA 193 chr7 ENST00000005180.8 CCL26 CCAGUAACAGCUGCUCCCAG 194 chr7 ENST00000005180.8 CCL26 GUAUUGGAAGCAGCAGGUCU 195 chr7 ENST00000005180.8 CCL27 GAGCUCACACGAAAGCCUGG 196 chr9 ENST00000259631.4 CCL27 ACUGAGGAAGGUCAUCCAGG 197 chr9 ENST00000259631.4 CCL27 AGGCAGUGCUGGGUGGCAGU 198 chr9 ENST00000259631.4 CCL28 AAUCCUUCCAGCACAGAUUU 199 chr5 ENST00000361115.4 CCL28 GUGCCCCCACUCACCUUCUG 200 chr5 ENST00000361115.4 CCL28 CAGGCAGGAAUGCAGCAGAG 201 chr5 ENST00000361115.4 CCL3 GCCACAAGAAAAGAUUGAUG 202 chr17 ENST00000613922.1 CCL3 ACUCACGUGAUGCAGAGAAC 203 chr17 ENST00000613922.1 CCL3 UCACCUGCUCAGAAUCAUGC 204 chr17 ENST00000613922.1 CCL4* UGAGAGCGCUGGAGAGCAGA 205 chr17 ENST00000615863.1 CCL4* UGAGAGCGCUGGAGAGCAGA 206 chr17 ENST00000615863.1 CCL4* UGAGAGCGCUGGAGAGCAGA 207 chr17 ENST00000615863.1 CCL5 GACUCACACGACUGCUGGGU 208 chr17 ENST00000603197.5 CCL5 UGAUGUGGGCACGGGGCAGU 209 chr17 ENST00000603197.5 CCL5 CUUUCCUCUUCCAGAUUCCU 210 chr17 ENST00000603197.5 CCL7 AUUGAUAAAUCUGUAGCAGC 211 chr17 ENST00000378569.2 CCL7 CCACAUACAUUACAGCUUCC 212 chr17 ENST00000378569.2 CCL7 CUAGUCCUAUUCCCUGCCCA 213 chr17 ENST00000378569.2 CCL8* AAAGCAGCAGGUGAUUGGAA 214 chr17 ENST00000394620.1 CCL8* CACCAACAUCCAAUGUCCCA 215 chr17 ENST00000394620.1 CCL8* CCCCCAUUCAAAAGUUCUGA 216 chr17 ENST00000394620.1 CCR1 CCUGGUUGGAAACAUCCUGG 217 chr3 ENST00000296140.3 CCR1 AGGCCCUCUCGUUCACCUUC 218 chr3 ENST00000296140.3 CCR1 UCAUAGUCCUCUGUGGUGUU 219 chr3 ENST00000296140.3 CCR2 GAUAAACCGAGAACGAGAUG 220 chr3 ENST00000445132.2 CCR2 ACCUUUUUUGAUUAUGAUUA 221 chr3 ENST00000445132.2 CCR2 GUAGAGCGGAGGCAGGAGUU 222 chr3 ENST00000445132.2 CCR3 CUAGAUACAGUUGAGACCUU 223 chr3 ENST00000357422.2 CCR3 UAUCAGCUUUUUCACAGAGC 224 chr3 ENST00000357422.2 CCR3 GGUGUUCACUGUGGGCCUCU 225 chr3 ENST00000357422.2 CCR5 UUUUGCAGUUUAUCAGGAUG 226 chr3 ENST00000292303.4 CCR5 AAAACAGGUCAGAGAUGGCC 227 chr3 ENST00000292303.4 CCR5 UGUAUUUCCAAAGUCCCACU 228 chr3 ENST00000292303.4 CCR6 UUGUUCUUACUCUCCCAUUC 229 chr6 ENST00000341935.9 CCR6 GCCUUUUAGCAACUUGCACG 230 chr6 ENST00000341935.9 CCR6 CCGGUACAUCGCCAUUGUAC 231 chr6 ENST00000341935.9 CCR7 GGCCGCGCUGUAGGCCCAGA 232 chr17 ENST00000246657.2 CCR7 GAGCAGGUAGGUAUCGGUCA 233 chr17 ENST00000246657.2 CCR7 UAGGCCCACGAAACAAAUGA 234 chr17 ENST00000246657.2 CD109 UCCGGGCCUGAUGAUCCCUG 235 chr6 ENST00000287097.5 CD109 GCCUUCACAGUCACCUGUGA 236 chr6 ENST00000287097.5 CD109 CAAAGACUCCUUCUGCUUCC 237 chr6 ENST00000287097.5 CD27** CCUUCACGAGGAAUGUUCCU 238 chr12 ENST00000266557.3 CD27** UCCUUCACGAGGAAUGUUCC 239 chr12 ENST00000266557.3 CD27** GCUGGUCACAGUCCUUCACG 240 chr12 ENST00000266557.3 CD27** ACUGAGCAGCCUUUCUAUGC 241 chr12 ENST00000266557.3 CD28*** CACCAAAAUCUUGUUUCCUG 242 ch2 ENST00000458610.6 CD28*** UCACCAAAAUCUUGUUUCCU 243 ch2 ENST00000458610.6 CD28*** UUGUCGUACGCUACAAGCAU 244 ch2 ENST00000458610.6 CD28*** AUUGUCGUACGCUACAAGCA 245 ch2 ENST00000458610.6 CD36 CAAGAAAAAUGGGCUGUGAC 246 chr7 ENST00000309881.11 CD36 GGUGCUGUCCUGGCUGUGUU 247 chr7 ENST00000309881.11 CD36 UAUCCAGAAGACAAUUAAAA 248 chr7 ENST00000309881.11 CD4** AGUGCAAUGUAGGAGUCCAA 249 chr12 ENST00000011653.8 CD4** CUGGAGCUCCAGCUGAGACA 250 chr12 ENST00000011653.8 CD4** UUUUGAACUCCACCUUCUUC 251 chr12 ENST00000011653.8 CD40LG** CAAAAUAGAUAGAAGAUGAA 252 chrX ENST00000370629.6 CD40LG** ACGAUACAGAGAUGCAACAC 253 chrX ENST00000370629.6 CD40LG** CCAGUUUGAAGGCUUUGUGA 254 chrX ENST00000370629.6 CD70 AGCGCUGGAUGCACACCACG 255 chr19 ENST00000245903.3 CD70 AGCCCGCAGGACGCACCCAU 256 chr19 ENST00000245903.3 CD70 CGCCGCGGCGAUGCCGGAGG 257 chr19 ENST00000245903.3 CD74 UGCUCACACAUACCUCUCCG 258 chr5 ENST00000009530.11 CD74 UGUUGGAGAUAAGGUCGCGC 259 chr5 ENST00000009530.11 CD74 AGAUGCACAGGAGGAGAAGC 260 chr5 ENST00000009530.11 CD8A** CCGGAACUGGCUCGGCCUGG 261 ch2 ENST00000409511.6 CD8A** CACCCGGAACUGGCUCGGCC 262 ch2 ENST00000409511.6 CD8A** GGCGACACCCGGAACUGGCU 263 ch2 ENST00000409511.6 CD8A** CGCCAGGCCGAGCCAGUUCC 264 ch2 ENST00000409511.6 CER1 GGCACUGCGACAAACAGAUC 265 chr9 ENST00000380911.3 CER1 AAAGAGAACUCUGAUUCUGG 266 chr9 ENST00000380911.3 CER1 CUGCUGGUACUCCUGCCUCU 267 chr9 ENST00000380911.3 CHRD GCCGGCGGGGCCGGGAGGCU 268 chr3 ENST00000204604.5 CHRD UCCCGGCCGGCCCGCGGCGC 269 chr3 ENST00000204604.5 CHRD CUGCCCGUUCGGGGAGCGGC 270 chr3 ENST00000204604.5 CKLF GUGAUAACAAUAUAUGGUUC 271 chr16 ENST00000264001.8 CKLF GACUUGAUCGAUUAAUGAAG 272 chr16 ENST00000264001.8 CKLF GUAGGAAAAAGUAAAAUUUA 273 chr16 ENST00000264001.8 CLCF1 CAUAGGUCCCAGCCAAGCUG 274 chr11 ENST00000312438.7 CLCF1 CAUAGGUUUUCUGGAUGGAG 275 chr11 ENST00000312438.7 CLCF1 GGUGCCAGAGCACCGUGCAC 276 chr11 ENST00000312438.7 CMTM1 GACUCAGGUUUGGCGUGUUC 277 chr16 ENST00000379500.6 CMTM1 UACGCUGCCGCUACUUGCCA 278 chr16 ENST00000379500.6 CMTM1 UGCGGGGUGCUUCCGGGGUG 279 chr16 ENST00000379500.6 CMTM2 CGAGUCAGUCAUGGCACCUA 280 chr16 ENST00000268595.2 CMTM2 UCCACCCGGGGCCAAACCCG 281 chr16 ENST00000268595.2 CMTM2 AAAGGCGGUGCAGGACCAUA 282 chr16 ENST00000268595.2 CMTM3 CCGGACCCCGAGCCUGCCGG 283 chr16 ENST00000361909.8 CMTM3 GGAAAGCCCGCGCCGGCAGC 284 chr16 ENST00000361909.8 CMTM3 UCCCGCCGCACUCACCGACU 285 chr16 ENST00000361909.8 CMTM4 CCGCCCGGCACCUACCACUU 286 chr16 ENST00000394106.6 CMTM4 GGUAGUCGGGGUCGCAGCGC 287 chr16 ENST00000394106.6 CMTM4 GCUGCUGGCGCCCGAGAUCA 288 chr16 ENST00000394106.6 CMTM5 GCUCAGUGCUCGAGAUCGCC 289 chr14 ENST00000359320.7 CMTM5 CCAGGGCUUCGCGGUGGACA 290 chr14 ENST00000359320.7 CMTM5 UUACCAGCUCGGUUUCCAGC 291 chr14 ENST00000359320.7 CMTM6 UUGAGAACGCGCCGGAGCAA 292 chr3 ENST00000205636.3 CMTM6 CGCUCCGGGGGCCUCUGGCG 293 chr3 ENST00000205636.3 CMTM6 CGGCCCGAGGCGAUGGAGAA 294 chr3 ENST00000205636.3 CMTM7 GGAGCUCCGCACACAGAUGA 295 chr3 ENST00000334983.9 CMTM7 AAUGAUCCUCGCCUUUUACC 296 chr3 ENST00000334983.9 CMTM7 CGACAGGGGCCAGCUGAUAC 297 chr3 ENST00000334983.9 CMTM8 GUGUGCGAGCGGGCGCGCUG 298 chr3 ENST00000307526.3 CMTM8 CAGCAGCUUCGCCUACGACC 299 chr3 ENST00000307526.3 CMTM8 CCCGUCGGCACUCACGAUCU 300 chr3 ENST00000307526.3 CNTF AUCAACCUGGACUCUGCGGA 301 chr11 ENST00000361987.5 CNTF GGAAGGUACGAUAAGCUUGA 302 chr11 ENST00000361987.5 CNTF GUGCAUUUUACCCCAACCGA 303 chr11 ENST00000361987.5 CNTFR CCAGCUGAGAGCCGUUGAGC 304 chr9 ENST00000351266.8 CNTFR GGGAUGCUGCGGUGACGUGG 305 chr9 ENST00000351266.8 CNTFR CAGGCGCUCGUACUGCACAU 306 chr9 ENST00000351266.8 COPS5 UAGUCCAGGGCUUCGCCGCC 307 chr8 ENST00000357849.8 COPS5 CUGAGCUUCCUGCAUGUUGU 308 chr8 ENST00000357849.8 COPS5 CCUCGGCGAUGGCGGCGUCC 309 chr8 ENST00000357849.8 CRLF1 CCAGCGUGAGUACAUCGGAG 310 chr19 ENST00000392386.7 CRLF1 CAUAGGGCGUAAAGAGAGCC 311 chr19 ENST00000392386.7 CRLF1 ACUCCUCACAUGUGUUGUCC 312 chr19 ENST00000392386.7 CSF1* GCCUUCUUAAGGUAGCACAC 313 chr1 ENST00000329608.10 CSF1* GGUGUUAUCUCUGAAGCGCA 314 chr1 ENST00000329608.10 CSF1* GUCAUGCUCUUCAUAAUCCU 315 chr1 ENST00000329608.10 CSF1R CACCUUUCUGCACUUUCAGC 316 chr5 ENST00000286301.7 CSF1R CAAUGCAGUGCCCUGAUGGG 317 chr5 ENST00000286301.7 CSF1R CCAGGGCGAGAAGGAGUAGU 318 chr5 ENST00000286301.7 CSF2* CCACAGUGCCCAAGAGCAGC 319 chr5 ENST00000296871.3 CSF2* CAGGGCUGCGUGCUGGGGCU 320 chr5 ENST00000296871.3 CSF2* UAGAGACACUGCUGCUGAGA 321 chr5 ENST00000296871.3 CSF3 UGUGCCACAGCAGCAGCUGC 322 chr17 ENST00000225474.6 CSF3 GAAGCUCUGGGGCAGGGAGC 323 chr17 ENST00000225474.6 CSF3 GGGCGAUGGCGCAGCGCUCC 324 chr17 ENST00000225474.6 CSF3R GCAAUAGCAACAAGACCUGG 325 chr1 ENST00000361632.8 CSF3R AUAGCCCUGAGGCCAUGGAU 326 chr1 ENST00000361632.8 CSF3R GCAUGGAGUCUGGUCAGAGC 327 chr1 ENST00000361632.8 CTF1 UCUCCGCAGGUGCAGCUCCA 328 chr16 ENST00000279804.2 CTF1 CCGGCCACCGGCAGCCGCGG 329 chr16 ENST00000279804.2 CTF1 AGCCGCAGCCGCUCGUGCAC 330 chr16 ENST00000279804.2 CX3CL1 GUGCCGACCCGAAGGAGCAA 331 chr16 ENST00000006053.6 CX3CL1 CUUCGAGAAGCAGAUCGGCG 332 chr16 ENST00000006053.6 CX3CL1 CGCCUGUGGCUUCGGGCUCC 333 chr16 ENST00000006053.6 CX3CR1** CUACCAACAAAUUUCCCACC 334 chr3 ENST00000399220.2 CX3CR1** UUGGGGACAUCGUGGUCUUU 335 chr3 ENST00000399220.2 CX3CR1** AAGUUUUCUGUCACUGAUUC 336 chr3 ENST00000399220.2 CXCL1 GGAGAGAGCAGCGCGGGCCA 337 chr4 ENST00000395761.3 CXCL1 CUGGCCGGCGCGCAGCAGGU 338 chr4 ENST00000395761.3 CXCL1 GUGCCUACCCCAGCCGCGUC 339 chr4 ENST00000395761.3 CXCL10 UACAGUAUAUAAUUACAACC 340 chr4 ENST00000306602.2 CXCL10 CGUGGACAAAAUUGGCUUGC 341 chr4 ENST00000306602.2 CXCL10 UUGAUUACUAAUGCUGAUGC 342 chr4 ENST00000306602.2 CXCL11 GCUGAAGAUGACAAUGGUGC 343 chr4 ENST00000306621.7 CXCL11 GUUGUUACUUGGGUACAUUA 344 chr4 ENST00000306621.7 CXCL11 AGCGUCCUCUUUUGAACAUG 345 chr4 ENST00000306621.7 CXCL12 CUACACCUUUAAUAAGACUC 346 chr10 ENST00000343575.10 CXCL12 UCAAGACUUACACAAUCUGA 347 chr10 ENST00000343575.10 CXCL12 UGACGUUGGCUCUGGCAACA 348 chr10 ENST00000343575.10 CXCL13 AGGUCUAUUACACAAGCUUG 349 chr4 ENST00000286758.4 CXCL13 UUCGAUCAAUGAAGCGUCUA 350 chr4 ENST00000286758.4 CXCL13 ACUUACAUGAUUUCUUUUCU 351 chr4 ENST00000286758.4 CXCL14 AAUUGGCGCUUGGGUUCCCC 352 chr5 ENST00000337225.5 CXCL14 CUGUACACCGCGCGUGUGGA 353 chr5 ENST00000337225.5 CXCL14 GAGGGGCGCGGCGUGGGAGC 354 chr5 ENST00000337225.5 CXCL16 GCGCUGAGUGGACUGCAAGG 355 chr17 ENST00000293778.10 CXCL16 UACCAGCCCCCCAAUUUCUC 356 chr17 ENST00000293778.10 CXCL16 AAUGUGGACAUGCUUACUCG 357 chr17 ENST00000293778.10 CXCL17 AUUGGUCUCAGAGGGGCCCA 358 chr19 ENST00000601181.5 CXCL17 GACCUUUGCACUCACAUUCU 359 chr19 ENST00000601181.5 CXCL17 CUUCCGACAGGGGUCGCCAG 360 chr19 ENST00000601181.5 CXCL2 GCAGUGGCAGCGGCAGCGAU 361 chr4 ENST00000508487.2 CXCL2 UUCUUCCCUAGGAGCGCCCC 362 chr4 ENST00000508487.2 CXCL2 UUCUUCCCUAGGAGCGCCCC 363 chr4 ENST00000508487.2 CXCL3* UGGCAGCGGAAGCGCGGGGC 364 chr4 ENST00000296026.4 CXCL3* GGGACCUUACAUUCACACUU 365 chr4 ENST00000296026.4 CXCL3* GGGACCUUACAUUCACACUU 366 chr4 ENST00000296026.4 CXCL5 CCCUUUAUAGGGCAGGUUGC 367 chr4 ENST00000296027.4 CXCL5 GCGCCAUGCGCUCUCACCGC 368 chr4 ENST00000296027.4 CXCL5 GAGCUCCUUGUGCGCGCUGU 369 chr4 ENST00000296027.4 CXCL6* GCCCGAAGGACCCGGGACAC 370 chr4 ENST00000226317.9 CXCL6* GGGGCCCCGGCGGCGUCAGC 371 chr4 ENST00000226317.9 CXCL6* UUUUUAUAGGGCAGGUUGCU 372 chr4 ENST00000226317.9 CXCL8 CAACAGGUGCAGUUUUGCCA 373 chr4 ENST00000307407.7 CXCL8 AAAUUUGGGGUGGAAAGGUU 374 chr4 ENST00000307407.7 CXCL8 UACUUACAUAAUUUCUGUGU 375 chr4 ENST00000307407.7 CXCL9* UUUCAAUUUUCUCGCAGGAA 376 chr4 ENST00000264888.5 CXCL9* AUUGUAGGUGGAUAGUCCCU 377 chr4 ENST00000264888.5 CXCL9* GGAACCCCAGUAGUGAGAAA 378 chr4 ENST00000264888.5 CXCR1 GAUGGUAAGCCUGGCGGAAA 379 chr2 ENST00000295683.2 CXCR1 UUGGUCAAGUUUGUUUGUCU 380 chr2 ENST00000295683.2 CXCR1 CUACAGUGGCAUCCUGCUGU 381 chr2 ENST00000295683.2 CXCR2 GUGACAGCUUUGAAGAUUUC 382 chr2 ENST00000318507.6 CXCR2 AUCUAGUAGAAAAGGGGGCA 383 chr2 ENST00000318507.6 CXCR2 UGUGGUCAUUAUCUAUGCCC 384 chr2 ENST00000318507.6 CXCR3{circumflex over ( )} GCAGAAAGAGGAGGCUGUAG 385 chrX ENST00000373693.3 CXCR3{circumflex over ( )} UACCUCCCCGCCCUGCCCAC 386 chrX ENST00000373693.3 CXCR3{circumflex over ( )} AAGAGCUGAAGUUCUCCAGG 387 chrX ENST00000373693.3 CXCR4{circumflex over ( )} CCCAAAGUACCAGUUUGCCA 388 chr2 ENST00000409817.1 CXCR4{circumflex over ( )} AGAGGAGGUCGGCCACUGAC 389 chr2 ENST00000409817.1 CXCR4{circumflex over ( )} UGGAUUGGUCAUCCUGGUCA 390 chr2 ENST00000409817.1 CXCR6** GGAAGUCUUGAUGCUCCUCC 391 chr3 ENST00000304552.4 CXCR6** GGUGUUUGUCUGUGGUCUGG 392 chr3 ENST00000304552.4 CXCR6** CCGUCAGGCUCUGCAACUUA 393 chr3 ENST00000304552.4 EBB CACCCUGUGCAGGCUCGGCA 394 chr19 ENST00000221847.5 EBB GGAUGUCCAGCUGUUCUCCA 395 chr19 ENST00000221847.5 EBB AGCUGCUGCUGGAGCCCCAG 396 chr19 ENST00000221847.5 EDN1 UUUCUCUCCCCAGCAGUCUU 397 chr6 ENST00000379375.5 EDN1 CCACUCCCAGUCCACCCUGG 398 chr6 ENST00000379375.5 EDN1 UCUGCCACCUGGACAUCAUU 399 chr6 ENST00000379375.5 ELANE CACAAUCUCCGAGGCCAGCG 400 chr19 ENST00000263621.1 ELANE GUGUCCCUGCAGCUGCGCGG 401 chr19 ENST00000263621.1 ELANE GCGGCCGACAUGACGAAGUU 402 chr19 ENST00000263621.1 ENG CCGGGCCACUCGGCCGGGUA 403 chr9 ENST00000344849.4 ENG CGCCUUCCAAGUGGCAGCCC 404 chr9 ENST00000344849.4 ENG CGUGCGGCCCAUGUCCUGGC 405 chr9 ENST00000344849.4 EPO CUGUUCUAGAAUGUCCUGCC 406 chr7 ENST00000252723.2 EPO CCCUCUGGGCCUCCCAGUCC 407 chr7 ENST00000252723.2 EPO CCUGGAGAGGUACCUCUUGG 408 chr7 ENST00000252723.2 FAM3B UUACAGCUCCAGUCCCCAAA 409 chr21 ENST00000357985.6 FAM3B UGUAGGCAUAGGUGUCAGAU 410 chr21 ENST00000357985.6 FAM3B GUUAUCCUCAAAGCAGAUUU 411 chr21 ENST00000357985.6 FAM3C CUGAUAGUGCAUUUUACUUU 412 chr7 ENST00000359943.7 FAM3C AUUGUUCUUACCAUUUGCCA 413 chr7 ENST00000359943.7 FAM3C UCCCCCUUCAGUUUAAUGAG 414 chr7 ENST00000359943.7 FAM3D GUGUCUUAGGUACUUACAUG 415 chr3 ENST00000358781.6 FAM3D UUUGCGUUUAAAAUCUGCAG 416 chr3 ENST00000358781.6 FAM3D GAGGUUAAAAAGUACAAGUG 417 chr3 ENST00000358781.6 FAS CACUUGGGCAUUAACACUUU 418 chr10 ENST00000355740.6 FAS UACAGUUGAGACUCAGAACU 419 chr10 ENST00000355740.6 FAS GUGUAACAUACCUGGAGGAC 420 chr10 ENST00000355740.6 FASLG UGGGGAUAUGGGUAAUUGAA 421 chr1 ENST00000367721.2 FASLG AACUGUGCCUGGAGGGGCCC 422 chr1 ENST00000367721.2 FASLG GGUGGUGGCCUCCUUUGACC 423 chr1 ENST00000367721.2 FGF2 CCGCAGGGACCAUGGCAGCC 424 chr4 ENST00000608478.1 FGF2 GGGUCCUUGAAGUGGCCGGG 425 chr4 ENST00000608478.1 FGF2 ACGGCCGAGUUGACGGGGUC 426 chr4 ENST00000608478.1 FLT3LG CUCUAGGAGGAGCUCUGCGG 427 chr19 ENST00000594009.5 FLT3LG GAGCGGCUCAAGACUGUCGC 428 chr19 ENST00000594009.5 FLT3LG GCUGACCUGAAAGGCACAUU 429 chr19 ENST00000594009.5 FOXP3 AGGACCCGAUGCCCAACCCC 430 chrX ENST00000376207.8 FOXP3 CCGAGGGCUUGCCAGGCCUG 431 chrX ENST00000376207.8 FOXP3 CCGAUGCCCAACCCCAGGCC 432 chrX ENST00000376207.8 FOXP3 CCCCAGGCCUGGCAAGCCCU 433 chrX ENST00000376207.8 FZD4 UCGUCCCCGAAGCCCCGCGC 434 chr11 ENST00000531380.1 FZD4 CAGACUGAGACCGACGCCCC 435 chr11 ENST00000531380.1 FZD4 CGAUGCUGGCCAUGGCCUGG 436 chr11 ENST00000531380.1 GATA3 GAGCACAGCCGAGGCCAUGG 437 chr10 ENST00000346208.4 GATA3 CUGGUCCGCCGUCACCUCCA 438 chr10 ENST00000346208.4 GATA3 AGCCGAGGCCAUGGAGGUGA 439 chr10 ENST00000346208.4 GATA3 CGAGGCCAUGGAGGUGACGG 440 chr10 ENST00000346208.4 GBP1 UCCUCACAUCUUCAUAAUGG 441 chr1 ENST00000370473.4 GBP1 CAAGCUGGCUGGAAAGAAAA 442 chr1 ENST00000370473.4 GBP1 UUCUGCCAUUACACAGCCUA 443 chr1 ENST00000370473.4 GDF1 CGUCCGCCGCGAGCCAGACC 444 chr19 ENST00000247005.7 GDF1 GGCCGGUUCCCCCGGUCAUG 445 chr19 ENST00000247005.7 GDF1 GGGGCACGGGGGCGCGGGUC 446 chr19 ENST00000247005.7 GDF10 CCAUGGCUCAUGUCCCCGCU 447 chr10 ENST00000580279.1 GDF10 CGUUGUUUCUGCUGUUGCUC 448 chr10 ENST00000580279.1 GDF10 CGCGGGCAGUGCGGACCAGG 449 chr10 ENST00000580279.1 GDF11 ACGGGGCAGCCGUCCGGCUC 450 chr12 ENST00000257868.9 GDF11 UCUGCGACUUGAUGCUCUCU 451 chr12 ENST00000257868.9 GDF11 CACCACCUCGCGGCUGAUGU 452 chr12 ENST00000257868.9 GDF15 CACCGUCCUGAGUUCUUGCC 453 chr19 ENST00000252809.3 GDF15 GCUCGCCUCGGCCAGAGACA 454 chr19 ENST00000252809.3 GDF15 CUCUCGGAAUCUGGAGUCUU 455 chr19 ENST00000252809.3 GDF2 GCGGGCCUAAGAUGUGUCCU 456 chr10 ENST00000581492.2 GDF2 CUGCAGUGGCUUCCCCUGUA 457 chr10 ENST00000581492.2 GDF2 AGGCACCCCCAGUGGGCUGU 458 chr10 ENST00000581492.2 GDF3 AAAAUUUUCUUCAAGAUAUA 459 chr12 ENST00000329913.3 GDF3 CCUUAUCUAAGCCCAGAAAU 460 chr12 ENST00000329913.3 GDF3 GUUAAUUCUGGCUUUGGGCC 461 chr12 ENST00000329913.3 GDF5 CCCUGGCCUGAAGACGUUCC 462 chr20 ENST00000374369.7 GDF5 UGACUUGGGCCAGAGACCCC 463 chr20 ENST00000374369.7 GDF5 GGUACCAAAGCAAGAAAGUG 464 chr20 ENST00000374369.7 GDF6 GCGGCUUCGCAUGCCCUUGG 465 chr8 ENST00000287020.6 GDF6 GGAUUUGCCCGGUUUCCAGC 466 chr8 ENST00000287020.6 GDF6 GCCCGCCAUGGAUACUCCCA 467 chr8 ENST00000287020.6 GDF7 AGCGCCUGCCGCCCCCGCGA 468 chr2 ENST00000272224.4 GDF7 GCUGGGCCGGUCCGGAGCCC 469 chr2 ENST00000272224.4 GDF7 UGCGGGCGCCGCGGCUGUCC 470 chr2 ENST00000272224.4 GDF9 AUACCUGUUACCUGGUCUCC 471 chr5 ENST00000378673.2 GDF9 AGAGCCGAACAGUGUUGUAG 472 chr5 ENST00000378673.2 GDF9 CUAUAAGACAUAUGCUACCA 473 chr5 ENST00000378673.2 GPI GUCCCGGGUGAGAGCGGCCA 474 chr19 ENST00000356487.9 GPI UCAGCUCGGAGCGGUGCUCG 475 chr19 ENST00000356487.9 GPI CGGCCCGCCCGCACCUGAAG 476 chr19 ENST00000356487.9 GREM1 UAUGAGCCGCACAGCCUACA 477 chr15 ENST00000622074.1 GREM1 CCCUUCAGCAGCCGGCAGCA 478 chr15 ENST00000622074.1 GREM1 UUGUGCUGGGCCUUGUCUGG 479 chr15 ENST00000622074.1 GREM2 CGGUGACCACCAGGGCCUCC 480 chr1 ENST00000318160.4 GREM2 GCAGCAACAACUCGGAGAGA 481 chr1 ENST00000318160.4 GREM2 GCUUUCCCUGUCCUUGUUCC 482 chr1 ENST00000318160.4 GRN CAGGCAGACCAUGUGGACCC 483 chr17 ENST00000053867.7 GRN GCUGGAACGCGGUGCCCAGA 484 chr17 ENST00000053867.7 GRN AGCUGGCUCCUCCGGGGUCC 485 chr17 ENST00000053867.7 HAX1 CACCUUUCUGCAGAACUUCC 486 chr1 ENST00000328703.11 HAX1 UACGGGAGGGACAGACACUU 487 chr1 ENST00000328703.11 HAX1 CCAGUCUGGUGCUGGUUGGG 488 chr1 ENST00000328703.11 HFE2 AGGAGCGGAGGGCUCGACAG 489 chr1 ENST00000336751.10 HFE2 UCAUCAGGAGCACUUCGAGG 490 chr1 ENST00000336751.10 HFE2 CGUACUCAGCAUUGCAGCGG 491 chr1 ENST00000336751.10 HMGB1* GAUACUCACGGAGGCCUCUU 492 chr13 ENST00000339872.8 HMGB1* GAUACUCACGGAGGCCUCUU 493 chr13 ENST00000339872.8 HMGB1* GAUACUCACGGAGGCCUCUU 494 chr13 ENST00000339872.8 HYAL2 GCGUGGGCCACAGUCCUGUG 495 chr3 ENST00000357750.8 HYAL2 UGCUGUGGGCUUGAGCUCCA 496 chr3 ENST00000357750.8 HYAL2 GCAGCCCCCAGCAUGCGGGC 497 chr3 ENST00000357750.8 ICAM3** UCAUGUUCCUGAAGGUGUCC 498 chr19 ENST00000160262.9 ICAM3** CAUGUUCCUGAAGGUGUCCA 499 chr19 ENST00000160262.9 ICAM3** AUGUUCCUGAAGGUGUCCAG 500 chr19 ENST00000160262.9 ICAM3** UCCUGAAGGUGUCCAGGGGC 501 chr19 ENST00000160262.9 ICOS** UUUUAUGCAGGAGAAAUCAA 502 ch2 ENST00000316386.10 ICOS** GAGAUGUUUAUAUUUCACAA 503 ch2 ENST00000316386.10 ICOS** AUGUUUAUAUUUCACAACGG 504 ch2 ENST00000316386.10 ICOS** UUUAAAAUGCAGUUGCUGAA 505 ch2 ENST00000316386.10 IFNA10 CAAACUCCUCCUGGGGGAUU 506 chr9 ENST00000357374.2 IFNA10 CAAACUCCUCCUGGGGGAUU 507 chr9 ENST00000357374.2 IFNA10 CAAACUCCUCCUGGGGGAUU 508 chr9 ENST00000357374.2 IFNA14 CAGGAGGACUUUGAUGCUCA 509 chr9 ENST00000380222.3 IFNA14 AAGCAAAGGGCAAUGCCAUU 510 chr9 ENST00000380222.3 IFNA14 AAGCAAAGGGCAAUGCCAUU 511 chr9 ENST00000380222.3 IFNA16 CAUCUCAUGGAAGGCAGAGA 512 chr9 ENST00000380216.1 IFNA16 AUAUGAUUUCGGAUUCCCCC 513 chr9 ENST00000380216.1 IFNA16 AUAUGAUUUCGGAUUCCCCC 514 chr9 ENST00000380216.1 IFNA2 UCAAGGUCCUCCUGCUACCC 515 chr9 ENST00000380206.3 IFNA2 CACCAGUAAAGCAAAGGUCA 516 chr9 ENST00000380206.3 IFNA2 CACCAGUAAAGCAAAGGUCA 517 chr9 ENST00000380206.3 IFNA5 UUGAUGAUAAUGGCACAAAU 518 chr9 ENST00000610521.1 IFNA5 CUUGCCCUUUGUUUUACUGA 519 chr9 ENST00000610521.1 IFNA5 CUUGCCCUUUGUUUUACUGA 520 chr9 ENST00000610521.1 IFNA6 AGGUCUGCUGAAUCACCUCA 521 chr9 ENST00000380210.1 IFNA6 ACAUGACUUCAGAUUUCCCC 522 chr9 ENST00000380210.1 IFNA6 UCAUGGUCCUCCUGUGACCC 523 chr9 ENST00000380210.1 IFNA8 UACAAGUCAUUCAGCUCUCU 524 chr9 ENST00000380205.1 IFNA8 GUUUAUCAUCAAACUCCUCC 525 chr9 ENST00000380205.1 IFNA8 GUUUAUCAUCAAACUCCUCC 526 chr9 ENST00000380205.1 IFNAR1 UUUACUUUAAAGAACUGGGA 527 chr21 ENST00000270139.7 IFNAR1 GAGUGAAGAAAAGUUGCAUU 528 chr21 ENST00000270139.7 IFNAR1 AAACACUUCUUCAUGGUAUG 529 chr21 ENST00000270139.7 IFNAR2 UAAACCAGAAGAUUUGAAGG 530 chr21 ENST00000342136.8 IFNAR2 UGAGUGGAGAAGCACACACG 531 chr21 ENST00000342136.8 IFNAR2 UCAGUUGCUCACACAAUUUC 532 chr21 ENST00000342136.8 IFNB1 UUGAAUACUGCCUCAAGGAC 533 chr9 ENST00000380232.3 IFNB1 GAAAAUUGCUGCUUCUUUGU 534 chr9 ENST00000380232.3 IFNB1 AGCACAACAGGAGAGCAAUU 535 chr9 ENST00000380232.3 IFNE UGGCCAGAGUGUGUCCUUUU 536 chr9 ENST00000448696.4 IFNE UAGACACUGCUGAAUUGACA 537 chr9 ENST00000448696.4 IFNE CUUGAUUCACUUGUCUUUGC 538 chr9 ENST00000448696.4 IFNG* UUUUUAAUAGUACUUGUUUG 539 chr12 ENST00000229135.3 IFNG* CUUCUUUUACAUAUGGGUCC 540 chr12 ENST00000229135.3 IFNG* GAAAUAUACAAGUUAUAUCU 541 chr12 ENST00000229135.3 IFNGR1** AUUGUACACCCUAAUGUAAC 542 chr6 ENST00000367739.8 IFNGR1** CUCCAUUUACAAAAACUGAA 543 chr6 ENST00000367739.8 IFNGR1** UUUCUGAUAUCCAGUUUAGG 544 chr6 ENST00000367739.8 IFNK UUGUGGCUUGAGAUCCUUAU 545 chr9 ENST00000276943.2 IFNK CGUUCAGUAAGUUACAGUCC 546 chr9 ENST00000276943.2 IFNK UUUUCUCGUAGACAUUCUAC 547 chr9 ENST00000276943.2 IFNL1 AUUUAGCCAUGGCUGCAGCU 548 chr19 ENST00000333625.2 IFNL1 GUGGCAGCCCUUCCCAGUUG 549 chr19 ENST00000333625.2 IFNL1 UAGCGAGCUUCAAGAAGGCC 550 chr19 ENST00000333625.2 IFNL3 CGGGCCUGUGUGAGUCGUCA 551 chr19 ENST0000041385L2 IFNL3 CCAAGACAUCCCCCAGGGCU 552 chr19 ENST0000041385L2 IFNL3 CCAAGACAUCCCCCAGGGCU 553 chr19 ENST0000041385L2 IFNW1 CUCCCUUUUACCAUCUCCUG 554 chr9 ENST00000380229.3 IFNW1 CAUUUGGUGCAGAAGCACCA 555 chr9 ENST00000380229.3 IFNW1 AGAUCCAACAGGGCUAUAGC 556 chr9 ENST00000380229.3 IL10* CGGAGAUCUCGAAGCAUGUU 557 chr1 ENST00000423557.1 IL10* UCAGACUGGGUGCCCUGGCC 558 chr1 ENST00000423557.1 IL10* CUCAGCACUGCUCUGUUGCC 559 chr1 ENST00000423557.1 IL10RA** GGUCUGGCUACAGUUGGAGA 560 chr11 ENST00000227752.7 IL10RA** GGUAGCCAUUGCUGUGGUAC 561 chr11 ENST00000227752.7 IL10RA** GGUGUUGGUGACGGUCCAGU 562 chr11 ENST00000227752.7 IL11 CGUGCCGCAGGUAGGACAGU 563 chr19 ENST00000264563.6 IL11 CGGCUCUAUCCCCAGCUCCC 564 chr19 ENST00000264563.6 IL11 CACUGGGAGCUCUACAGGUA 565 chr19 ENST00000264563.6 IL11RA AGUGUCCUGGUUUCGGGAUG 566 chr9 ENST00000318041.13 IL11RA GCUAGGGCAUGAACUGGUCC 567 chr9 ENST00000318041.13 IL11RA UGCCCCCAAGUGCACCAUCC 568 chr9 ENST00000318041.13 IL12A CCAGGGUAGCCACAAGGAGG 569 chr3 ENST00000305579.6 IL12A GGUCUGGAGUGGCCACGGGG 570 chr3 ENST00000305579.6 IL12A UGACGGCCCUCAGCAGGUUU 571 chr3 ENST00000305579.6 IL12B ACUCUUUGACUUGGAUGGUC 572 chr5 ENST00000231228.2 IL12B GGUGAUACCAUCUUCUUCAG 573 chr5 ENST00000231228.2 IL12B UUUAUGUCGUAGAAUUGGAU 574 chr5 ENST00000231228.2 IL12RB1{circumflex over ( )} CACUUCCUGCGGUGUUGGUG 575 chr19 ENST00000593993.6 IL12RB1{circumflex over ( )} GGAGCACUCGUAACGAUCAC 576 chr19 ENST00000593993.6 IL12RB1{circumflex over ( )} AUCUCUUCCAGGCUCGGCCU 577 chr19 ENST00000593993.6 IL13* CAUGGCGCUUUUGUUGACCA 578 chr5 ENST00000304506.7 IL13* GCCUCCCUCUACAGCCCUCA 579 chr5 ENST00000304506.7 IL13* CGACACUCACCUUCUGGUUC 580 chr5 ENST00000304506.7 IL15 AUGGAAAUACUUCUCAAAUG 581 chr4 ENST00000296545.11 IL15 GGCAUUCAUGUCUUCAUUUU 582 chr4 ENST00000296545.11 IL15 AUGGUCAUGAUGAUUGUCCU 583 chr4 ENST00000296545.11 IL16 CAAAAUUUCGGUCCAUCUCC 584 chr15 ENST00000302987.8 IL16 AGGGCUAGAGCCAUCAUCAC 585 chr15 ENST00000302987.8 IL16 GGAAAAUUCCCUCCUUGCCC 586 chr15 ENST00000302987.8 IL17A{circumflex over ( )} GCUACUGCUGCUGAGCCUGG 587 chr6 ENST00000340057.1 IL17A{circumflex over ( )} UCAACCUGAACAUCCAUAAC 588 chr6 ENST00000340057.1 IL17A{circumflex over ( )} GGAUCGGUUGUAGUAAUCUG 589 chr6 ENST00000340057.1 IL17B{circumflex over ( )} GCUCUGAGCUGUUCCUCAGC 590 chr5 ENST00000261796.3 IL17B{circumflex over ( )} GAAACCGUAUGCCCGCAUGG 591 chr5 ENST00000261796.3 IL17B{circumflex over ( )} CUCUUGCUUUUGGGGCUCCU 592 chr5 ENST00000261796.3 IL17C{circumflex over ( )} UCAGAAACAGGAGGCCGGGG 593 chr16 ENST00000244241.4 IL17C{circumflex over ( )} CGGUACCCCACACUGCUACU 594 chr16 ENST00000244241.4 IL17C{circumflex over ( )} GCACCUCGAGCCAGCAGGUG 595 chr16 ENST00000244241.4 IL17D{circumflex over ( )} CGGCAGCGCCAGCAGGAAGC 596 chr13 ENST00000304920.3 IL17D{circumflex over ( )} GGACCGGCCGGAGGAGCUAC 597 chr13 ENST00000304920.3 IL17D{circumflex over ( )} GUGGAAGGCACUGAGCACGC 598 chr13 ENST00000304920.3 IL17F{circumflex over ( )} GGUAGUAUGAAGCUUGACAU 599 chr6 ENST00000336123.4 IL17F{circumflex over ( )} GAAAAAAGUAUGUCCUACUU 600 chr6 ENST00000336123.4 IL17F{circumflex over ( )} UACUUGCUGCUGUCGAUAUU 601 chr6 ENST00000336123.4 IL18 GGAAAUAAUUUUGUUCUCAC 602 chr11 ENST00000280357.11 IL18 UUACAGCCAUACCUCUAGGC 603 chr11 ENST00000280357.11 IL18 UUAUUUCAGAUAAUGCACCC 604 chr11 ENST00000280357.11 IL18BP GCAGGACCCACAAAGGGCUG 605 chr11 ENST00000260049.9 IL18BP UGUGCUUCUAACUGAGGCAG 606 chr11 ENST00000260049.9 IL18BP GCUGGACACUGCUUAGCUGC 607 chr11 ENST00000260049.9 IL19 AGUUACAGUGUGUUUCCCUU 608 chr1 ENST00000270218.10 IL19 CAGUAGACAACCACGGUCUC 609 chr1 ENST00000270218.10 IL19 CUUGGAAACUCUCUUCUAUA 610 chr1 ENST00000270218.10 IL1A GGAAGGUUCUGAAGAAGAGA 611 chr2 ENST00000263339.3 IL1A GGUAAGCUUGGAUGUUUUAG 612 chr2 ENST00000263339.3 IL1A GCCAUAGCUUACAUGAUAGA 613 chr2 ENST00000263339.3 IL1B* CAUUCUCCUGGAAGGUCUGU 614 chr2 ENST00000263341.6 IL1B* CAUGGCCACAACAACUGACG 615 chr2 ENST00000263341.6 IL1B* CUCUCCGCAGUGCUCCUUCC 616 chr2 ENST00000263341.6 IL1F10 AUCUGCAUACUUCCUAACAG 617 chr2 ENST00000341010.6 IL1F10 CCAGGCAGCGGCUCCCUCCC 618 chr2 ENST00000341010.6 IL1F10 GGCCUCUCACCUCCAGCUGU 619 chr2 ENST00000341010.6 IL1R1** UCCUUUUAAAGAUAAAUGCA 620 chr2 ENST00000410023.5 IL1R1** CUUAACCCAAAUGAACACAA 621 chr2 ENST00000410023.5 IL1R1** UAUCUACAGAACAAGCCUCC 622 chr2 ENST00000410023.5 IL1R2** CCAGAAGCUGCCGGUUUCGU 623 chr2 ENST00000332549.7 IL1R2** UGUAGCCCUGAGGUGCCCCC 624 chr2 ENST00000332549.7 IL1R2** UAAAAAUGACUCUGCUAGGA 625 chr2 ENST00000332549.7 IL1RAPL1** AAUUCUUAAGGAGCAUCUUG 626 chrX ENST00000378993.5 IL1RAPL1** CUCUGUGGAAGAAGGUGACU 627 chrX ENST00000378993.5 IL1RAPL1** UACACUCACCUCGUUUAUGA 628 chrX ENST00000378993.5 IL1RL1** UUUCUUAUUUCAGAAUUGUC 629 chr2 ENST00000233954.5 IL1RL1** AAUGUGAUGACUGAGGACGC 630 chr2 ENST00000233954.5 IL1RL1** ACCCUUGACCGUGAAGGACC 631 chr2 ENST00000233954.5 IL1RN** UUCCCCAGAAAAGAUAGAUG 632 chr2 ENST00000409930.3 IL1RN** ACAGGCACAUCUUCCCUCCA 633 chr2 ENST00000409930.3 IL1RN** AGCAUGUUUUUACCUCCAGC 634 chr2 ENST00000409930.3 IL2 UGUAAUAAUUUUAGUAAGAA 635 chr4 ENST00000226730.4 IL2 ACAACUGGAGCAUUUACUGC 636 chr4 ENST00000226730.4 IL2 GACUUAGUGCAAUGCAAGAC 637 chr4 ENST00000226730.4 IL20 AAGGCUGAAGGCAAGACUAG 638 chr1 ENST00000367096.7 IL20 UGGACUGAAGACACUCAAUU 639 chr1 ENST00000367096.7 IL20 UUCUGAGAUACGGGGCAGUG 640 chr1 ENST00000367096.7 IL20RA CAUCCCCGACCCGCACCUGG 641 chr6 ENST00000316649.9 IL20RA UGUUGCUCCUGGCGGCGCCU 642 chr6 ENST00000316649.9 IL20RA CCGCCGCCCAUGCGGGCUCC 643 chr6 ENST00000316649.9 IL20RB AGUGAGUGAGCACCAGCUGC 644 chr3 ENST00000329582.8 IL20RB UGCCAUACAACCUUCGUGUC 645 chr3 ENST00000329582.8 IL20RB UUCUAUUAAAGGGAUGCUUC 646 chr3 ENST00000329582.8 IL21 GAAAAAUUAUGUGAAUGACU 647 chr4 ENST00000264497.7 IL21 UCAUGUGGCGAUCUUGACCU 648 chr4 ENST00000264497.7 IL21 ACAAUCCUCUCCAUGUUGCC 649 chr4 ENST00000264497.7 IL22{circumflex over ( )} UGGACUUGUCAAGCCUGCAG 650 chr12 ENST00000328087.5 IL22{circumflex over ( )} UCUCUUGGCCCUCUUGGUAC 651 chr12 ENST00000328087.5 IL22{circumflex over ( )} AAGAGCUCACAGAUUUCUGC 652 chr12 ENST00000328087.5 IL22RA1{circumflex over ( )} GAUGUCUGGCUGCCCUAAGU 653 chr1 ENST00000270800.1 IL22RA1{circumflex over ( )} UCUGGACCCAGGGAGCCCGC 654 chr1 ENST00000270800.1 IL22RA1{circumflex over ( )} CAGGGAUCAGGACGUGCUCC 655 chr1 ENST00000270800.1 IL22RA2{circumflex over ( )} UUCUGAGUAGCUCCCAGCCG 656 chr6 ENST00000349184.8 IL22RA2{circumflex over ( )} CUGUAUGUCUGAGGUUUCAC 657 chr6 ENST00000349184.8 IL22RA2{circumflex over ( )} ACAGAUAUGGACAGAGACAA 658 chr6 ENST00000349184.8 IL23A* CUGCUGCCCUGGACAGCUCA 659 chr12 ENST00000228534.5 IL23A* AAGCUGCUGGCACUGAGUCC 660 chr12 ENST00000228534.5 IL23A* CUCACCAUGUGUCCCACUAG 661 chr12 ENST00000228534.5 IL23R** CUGUUGCACAUAUGUAAAAU 662 chr1 ENST00000347310.9 IL23R** GAUGUCAAGAAACAGGCAAA 663 chr1 ENST00000347310.9 IL23R** UAAGUACACUCACCUGUUUC 664 chr1 ENST00000347310.9 IL24 UGAGAGGCUGUCGCCAGCAA 665 chr1 ENST00000294984.6 IL24 CUUCUCUGGAGCCAGGUAUC 666 chr1 ENST00000294984.6 IL24 ACAACCCCCUUCACUUGGCA 667 chr1 ENST00000294984.6 IL25 CCUACAGGUGGUUGCAUUCU 668 chr14 ENST00000329715.2 IL25 GAGGUGUCCUGCCCUUUGCU 669 chr14 ENST00000329715.2 IL25 UGCCUCCCCUAGAGCCUGCU 670 chr14 ENST00000329715.2 IL26 AUAGAGAGCGUCAACAGCUU 671 chr12 ENST00000229134.4 IL26 AGAUUGCUUGUGCUUGGCAA 672 chr12 ENST00000229134.4 IL26 UGCUGGUGAAUUUCAUUUUG 673 chr12 ENST00000229134.4 IL27 CAUUAGGGGGACUUACAAAG 674 chr16 ENST00000356897.1 IL27 GCAGCUCCUGCAGGCUCAGC 675 chr16 ENST00000356897.1 IL27 ACCAGCUUGAACCAGGAGCA 676 chr16 ENST00000356897.1 IL2RA CAGAGCUUGUGCAUUGACAU 677 chr10 ENST00000379959.7 IL2RA GUGACCCGCUUUUUAUUCUG 678 chr10 ENST00000379959.7 IL2RA AUGGCUUUGAAUGUGGCGUG 679 chr10 ENST00000379959.7 IL2RB UGUGGCCUGGGGACAGCGUC 680 chr22 ENST00000216223.9 IL2RB CCCACAGAUGCAACAUAAGC 681 chr22 ENST00000216223.9 IL2RB GUUGUCUCCAGUUCGCCUGA 682 chr22 ENST00000216223.9 IL2RG CAUACCAAUAAUGCAGAGUG 683 chrX ENST00000374202.6 IL2RG UCGAGUACAUGAAUUGCACU 684 chrX ENST00000374202.6 IL2RG GAAACACUGAGGGAGUCAGU 685 chrX ENST00000374202.6 IL3* GCAGGAGCAGGACGGGCAGG 686 chr5 ENST00000296870.2 IL3* CAACGCCCUUGAAGACAAGC 687 chr5 ENST00000296870.2 IL3* CUACUCACCAGCAAAGGCAA 688 chr5 ENST00000296870.2 IL31 CUUUCAAAAGCAUCUUCGAG 689 chr12 ENST00000377035.1 IL31 GUAAACGGACGGGCAACGUG 690 chr12 ENST00000377035.1 IL31 AGAAAGAGCACAGACGUCGA 691 chr12 ENST00000377035.1 IL31RA CAACUUCGCUAAGAACCGUA 692 chr5 ENST00000447346.6 IL31RA AGCUCUGCGAUGUGCGGUCA 693 chr5 ENST00000447346.6 IL31RA CAGUCAUUCCCAUUUUUUCU 694 chr5 ENST00000447346.6 IL32 CUGCCUCUCUUCACAGCACC 695 chr16 ENST00000325568.9 IL32 AGAAUCAGGACGUGGACAGG 696 chr16 ENST00000325568.9 IL32 UCAGGGUGAGAAGGAUGAAG 697 chr16 ENST00000325568.9 IL33 UUGUUUAGAAUCCCAACAGA 698 chr9 ENST00000381434.7 IL33 CUCUGGCCUUAUGAUAAAAA 699 chr9 ENST00000381434.7 IL33 UUUCAGUGAAGGCCUUUUGG 700 chr9 ENST00000381434.7 IL34 UCUUGGGAUCUUCCUUGGCG 701 chr16 ENST00000288098.6 IL34 GCACUCCUCAUUCUGCGUCA 702 chr16 ENST00000288098.6 IL34 CAGGAGCCGACUUCAGUACA 703 chr16 ENST00000288098.6 IL36A CACAUGUCGGCAUGAGAUUA 704 chr2 ENST00000259211.6 IL36A GAUUGAGUCCAUUCAGGCCC 705 chr2 ENST00000259211.6 IL36A ACUCACCUUCAGCUGCAGUG 706 chr2 ENST00000259211.6 IL36B CAAGCCUACUUUGCAGCUUA 707 chr2 ENST00000327407.2 IL36B UAUGGUUUACCUGGGAAUCA 708 chr2 ENST00000327407.2 IL36B GCUAUUAAAUGAAGAGUGAC 709 chr2 ENST00000327407.2 IL36G UCAGUGUGUAAACCUAUUAC 710 chr2 ENST00000259205.4 IL36G CACAAGGUUCUGACCCUGAA 711 chr2 ENST00000259205.4 IL36G CUGUUUGCACUGCUGUGGCU 712 chr2 ENST00000259205.4 IL36RN CACAGGUGAAGAGAUCAGCG 713 chr2 ENST00000346807.7 IL36RN CACCCAGGAUGACGGGGGAC 714 chr2 ENST00000346807.7 IL36RN GGAGCCGACUCUAACACUAG 715 chr2 ENST00000346807.7 IL37 GCUAAUGCAAAGAAGAUCUC 716 chr2 ENST00000263326.7 IL37 AUUCUCCUGGGGGUCUCUAA 717 chr2 ENST00000263326.7 IL37 AACUCUCACCUUCAGCUGAA 718 chr2 ENST00000263326.7 IL4* CAGAGGGGGAAGCAGUUGGG 719 chr5 ENST00000231449.6 IL4* UGAUAUCGCACUUGUGUCCG 720 chr5 ENST00000231449.6 IL4* UACUCACCUUCUGCUCUGUG 721 chr5 ENST00000231449.6 IL5* CAUAAAGAAAAUUACCUCAU 722 chr5 ENST00000231454.5 IL5* UGCAUUGGUGAAAGAGACCU 723 chr5 ENST00000231454.5 IL5* CAUUUGAGUUUGCUAGCUCU 724 chr5 ENST00000231454.5 IL6* CCCUCCGGCACAGGCGCCUU 725 chr7 ENST00000258743.9 IL6* ACAUCUUUGGAAUCUUCUCC 726 chr7 ENST00000258743.9 IL6* AACGAAUUGACAAACAAAUU 727 chr7 ENST00000258743.9 IL6R** CAGUCCGGCCGAAGACUUCC 728 chr1 ENST00000368485.7 IL6R** UAACUGGCAGGAGAACUUCU 729 chr1 ENST00000368485.7 IL6R** CAGCAAAACUCAAACCUUUC 730 chr1 ENST00000368485.7 IL6ST AUUUACCUGGCUCCAAGUUG 731 chr5 ENST00000336909.9 IL6ST UUAUAACACUCUUAAUACUU 732 chr5 ENST00000336909.9 IL6ST UGAUAAAUUAUGUGGCGGAU 733 chr5 ENST00000336909.9 IL7 GGUCAGCAUCGAUCAAUUAU 734 chr8 ENST00000263851.8 IL7 AUGCUACUGGCAACAGAACA 735 chr8 ENST00000263851.8 IL7 UGUCAAAUUUAGUUUCUUUU 736 chr8 ENST00000263851.8 IL9{circumflex over ( )} CUACCUGCAUCUUGUUGAUG 737 chr5 ENST00000274520.1 IL9{circumflex over ( )} UGGACACCCCUGGCCUGCCA 738 chr5 ENST00000274520.1 IL9{circumflex over ( )} UGUCAAGAUGCUUCUGGCCA 739 chr5 ENST00000274520.1 INHA UCAGCAGCAAGAAGAGCAGU 740 chr2 ENST00000243786.2 INHA CCGGGAACUUGUUCUGGCCA 741 chr2 ENST00000243786.2 INHA CCGCGGUGACCAGGGAAGGU 742 chr2 ENST00000243786.2 INHBA UGAACUUAUGGAGCAGACCU 743 chr7 ENST00000242208.4 INHBA GAACGGGUAUGUGGAGAUAG 744 chr7 ENST00000242208.4 INHBA GGGUACCGGCUGGGUGACAU 745 chr7 ENST00000242208.4 INHBB GGCGGCGGCGCGGCAGGCGU 746 chr2 ENST00000295228.3 INHBB GUACGUCGUGCGGCGGCUUC 747 chr2 ENST00000295228.3 INHBB UGUGCCGCUUCACCGCCUCC 748 chr2 ENST00000295228.3 INHBC AAAGGCCAGAAGCAAUGAGG 749 chr12 ENST00000309668.2 INHBC UGGACACUGACCGCCAGCUC 750 chr12 ENST00000309668.2 INHBC GCGGGAGCUGCUUCUUGAUC 751 chr12 ENST00000309668.2 INHBE AAAAGUGAGCAGGGAGCUGU 752 chr12 ENST00000266646.2 INHBE CAAGCAAAGAGUGCCAGGAA 753 chr12 ENST00000266646.2 INHBE CCAGGAGAGUGCGGGACCCU 754 chr12 ENST00000266646.2 ITGA4** CCACCGAGAGCGCAUGGCUU 755 chr2 ENST00000397033.6 ITGA4** GACCGGCCGCCCCUACAACG 756 chr2 ENST00000397033.6 ITGA4** AGCCGAACAGCGUGUUGUGG 757 chr2 ENST00000397033.6 ITGAV** CGGCGAUGGCUUUUCCGCCG 758 chr2 ENST00000261023.7 ITGAV** GUCCCGAGAGAAGAAGCGGG 759 chr2 ENST00000261023.7 ITGAV** GACAGUCCUGCCGAGUACUC 760 chr2 ENST00000261023.7 ITGB1** UGCUGUUCCUUUGCUACGGU 761 chr10 ENST00000302278.7 ITGB1** GAUGACAUAGAAAAUCCCAG 762 chr10 ENST00000302278.7 ITGB1** AUUUAGACAUUUUUACAGGA 763 chr10 ENST00000302278.7 ITGB3** GCGAGGUGAGCCCAGAGGCA 764 chr17 ENST00000559488.5 ITGB3** AGGCCCGAGUACUAGAGGAC 765 chr17 ENST00000559488.5 ITGB3** GGGGACUGACUUGAGUGACC 766 chr17 ENST00000559488.5 KIT** CUCAACCAUCUGUGAGUCCA 767 chr4 ENST00000288135.5 KIT** AUCAGACUUAAUAGUCCGCG 768 chr4 ENST00000288135.5 KIT** AAAGUCCAUUUGACAAAGCC 769 chr4 ENST00000288135.5 KITLG UUUCUUUCACGCACUCCACA 770 chr12 ENST00000228280.9 KITLG AAGUUUUCAAAUAUUUCUGA 771 chr12 ENST00000228280.9 KITLG UCUUGCAGCCAAGUCAUUGU 772 chr12 ENST00000228280.9 KLHL20 GCACCGGGAGCUAUGUGAUG 773 chr1 ENST00000209884.4 KLHL20 UACUUCCGAGCUAUGUUUAC 774 chr1 ENST00000209884.4 KLHL20 UAGCCCUCUCGUCAAUGUCU 775 chr1 ENST00000209884.4 LEFTY1 GCUGCAGCAGGGCCACGUAC 776 chr1 ENST00000272134.5 LEFTY1 CCUCCAUGUCGGCCCUGUCC 777 chr1 ENST00000272134.5 LEFTY1 GUGUUGCCCCUGGCCAGCCC 778 chr1 ENST00000272134.5 LEFTY2 AUGUCGGCCCUGUCCAGUAC 779 chr1 ENST00000366820.9 LEFTY2 CUCCUCGGUCAGGGCCGCCC 780 chr1 ENST00000366820.9 LEFTY2 GCAGCACCAUGUGGCCCCUG 781 chr1 ENST00000366820.9 LIF GUCCCGGGUGAUGUUGCCCA 782 chr22 ENST00000249075.3 LIF UGCCGUUGGCGUGGAAGGGC 783 chr22 ENST00000249075.3 LIF UGUUGGGGAACGGCUCCCCC 784 chr22 ENST00000249075.3 LIFR UGAUGCACUUACCCUUUUUC 785 chr5 ENST00000263409.8 LIFR UAAAUGUUGAUAACAGCCAC 786 chr5 ENST00000263409.8 LIFR GAAACGACCAUCCUGGAUGG 787 chr5 ENST00000263409.8 LTA CCCUAGGGGCUCCCUGGUGU 788 chr6 ENST00000418386.2 LTA GAUGCAUCUUGGGGUGCUGA 789 chr6 ENST00000418386.2 LTA CAGGUGGAUGUUUACCAAUG 790 chr6 ENST00000418386.2 LTB UAUCACUGUCCUGGCUGUGC 791 chr6 ENST00000429299.2 LTB UCCCUCCUGCUAGCUGUGGC 792 chr6 ENST00000429299.2 LTB UUCAGUCUCAAUGGGGGCAC 793 chr6 ENST00000429299.2 LTBP1 AUGGUGGCCAGUGCAGUUCA 794 chr2 ENST00000407925.5 LTBP1 GUUUAGGCACGCUGGCACCA 795 chr2 ENST00000407925.5 LTBP1 GAGGCAAGGUAUGUGUUGAA 796 chr2 ENST00000407925.5 LTBP3 GCCCUCACCCACGCGGAAGC 797 chr11 ENST00000322147.8 LTBP3 AUGACGCUCAUCGGAGAGAA 798 chr11 ENST00000322147.8 LTBP3 CUGCAAGCGGACCUGUCUCA 799 chr11 ENST00000322147.8 LTBP4 CCCUUGAUCUGUCACAAUGG 800 chr19 ENST00000308370.11 LTBP4 GGCCGGGGGCCGGGCGCCCG 801 chr19 ENST00000308370.11 LTBP4 GUGCUCGUCGUCGCGGUGGU 802 chr19 ENST00000308370.11 MAF CAGGAGAAUGGCAUCAGAAC 803 chr16 ENST00000326043.4 MAF CAGGGGACUGGUGGGCAGGU 804 chr16 ENST00000326043.4 MAF UCCAUGGCCAGGGGACUGGU 805 chr16 ENST00000326043.4 MAF CGACCUGCCCACCAGUCCCC 806 chr16 ENST00000326043.4 MIF UUGGUGUUUACGAUGAACAU 807 chr22 ENST00000215754.7 MIF CAGCAGCUGGCGCAGGCCAC 808 chr22 ENST00000215754.7 MIF GCGCGGAACCCCUCGUCCGG 809 chr22 ENST00000215754.7 MINOS1- GGCCACGGGCAUGAUGCUUC 810 chr1 ENST00000602662.1 MINOS1- GAACAGUGCCAGCUUGUUGA 811 chr1 ENST00000602662.1 MINOS1- AGCCGCUGUGGCCCACGAUC 812 chr1 ENST00000602662.1 MSTN UGACGAUUAUCACGCUACAA 813 chr2 ENST00000260950.4 MSTN UUCCCGGAGUGGAGGAGCUU 814 chr2 ENST00000260950.4 MSTN AAUCCUCAGUAAACUUCGUC 815 chr2 ENST00000260950.4 NAMPT GCUGGGGACGAGCGCGCGGC 816 chr7 ENST00000222553.7 NAMPT CUUUACCUUGUAGGAGUCGG 817 chr7 ENST00000222553.7 NAMPT CCGGCCCGAGAUGAAUCCUG 818 chr7 ENST00000222553.7 NBL1 GGCCACGGGCAUGAUGCUUC 819 chr1 ENST00000375136.7 NBL1 GAACAGUGCCAGCUUGUUGA 820 chr1 ENST00000375136.7 NBL1 AGCCGCUGUGGCCCACGAUC 821 chr1 ENST00000375136.7 NDP UUGAGCUACACUUGUACAAU 822 chrX ENST00000378062.5 NDP CAGCUCAUUCAUAAUGGACU 823 chrX ENST00000378062.5 NDP CAGCAGGGAGAGCAUAGAAA 824 chrX ENST00000378062.5 NLRP7 GCCUCUUCCACCUCAGACCA 825 chr19 ENST00000328092.9 NLRP7 GAGUUUCAAAUCCCUUUUAU 826 chr19 ENST00000328092.9 NLRP7 CUGCAGAGUCCACUCUAGCU 827 chr19 ENST00000328092.9 NODAL UGACCAGGCCUCUCUCCAAG 828 chr10 ENST00000287139.7 NODAL GGGACAAAGUGACAGUGAAU 829 chr10 ENST00000287139.7 NODAL CUGUGUCGGGCUUUGGCUGG 830 chr10 ENST00000287139.7 NOG GACCACCACCAGGGCGUAGA 831 chr17 ENST00000332822.4 NOG GGCGGAUGUGGAGAUAGUGC 832 chr17 ENST00000332822.4 NOG UUGGGGUCAAAGAUAGGGUC 833 chr17 ENST00000332822.4 NRG1 GCUACAUCUACAUCCACCAC 834 chr8 ENST00000287842.7 NRG1 AAACUUUCUGUGUGAAUGGA 835 chr8 ENST00000287842.7 NRG1 UUACUUGCACAAGUAUCUCG 836 chr8 ENST00000287842.7 NRP1 UUGCAGAGCAGUGUCUCAGA 837 chr10 ENST00000265371.8 NRP1 GCUGUCGGUGUAAAAAACCA 838 chr10 ENST00000265371.8 NRP1 CCACAGUAACGCCCAAUGUG 839 chr10 ENST00000265371.8 NRP2 CUUUCAGACCCACCGUGCGG 840 chr2 ENST00000357785.9 NRP2 UCUGGUGGGAGGGGUAGUCC 841 chr2 ENST00000357785.9 NRP2 UUGAGGACAAUCUUCUGGUU 842 chr2 ENST00000357785.9 OSM AGGGCCCAGGUGCUUACAUA 843 chr22 ENST00000215781.2 OSM GAUCUGUCUGCUUCUGGAGC 844 chr22 ENST00000215781.2 OSM GUUUCCAAGCAUGGCGAGCA 845 chr22 ENST00000215781.2 OSMR AUUACAGCACCACUGUGAAG 846 chr5 ENST00000274276.7 OSMR CUUUGUAAGAAUAAAGAGUU 847 chr5 ENST00000274276.7 OSMR GAGCAACUGGAGUUCCUGGG 848 chr5 ENST00000274276.7 PARK7 UAGAUUAAGGUCACCGUUGC 849 chr1 ENST00000338639.9 PARK7 CAGGACAAAUGACCACAUCA 850 chr1 ENST00000338639.9 PARK7 CAUGGAGUUAUUCCUUCAUA 851 chr1 ENST00000338639.9 PDPN CAACUGCAAAGUUUGCUGUC 852 chr1 ENST00000294489.10 PDPN CCCCACCGUCGCGCUCCUCC 853 chr1 ENST00000294489.10 PDPN CAGCUCAGAAUCUUGCUGCU 854 chr1 ENST00000294489.10 PF4 UGUGAGGGCUGGCAGCGGCG 855 chr4 ENST00000296029.3 PF4 GUGGCAGGAGCAGCAACCCC 856 chr4 ENST00000296029.3 PF4 CGCAGCAUGAGCUCCGCAGC 857 chr4 ENST00000296029.3 PF4V1 GGCGCGGGUGAGGCGGGACC 858 chr4 ENST00000226524.3 PF4V1 AGAGCAGAAACCAGGCUGGG 859 chr4 ENST00000226524.3 PF4V1 AGAGCAGAAACCAGGCUGGG 860 chr4 ENST00000226524.3 PGLYRP1 CGAUACCACCACAUAGCGUA 861 chr19 ENST00000008938.4 PGLYRP1 CAGGGCCUUCCACUCGUUCC 862 chr19 ENST00000008938.4 PGLYRP1 GCCGCUCUAUGCUGCUUGCC 863 chr19 ENST00000008938.4 PLP2 ACCCUUCCAGAUAUUAUGCC 864 chrX ENST00000376327.5 PLP2 ACCGACAGGGAGGAGUAGCC 865 chrX ENST00000376327.5 PLP2 GGACCCCUUCUCACACUCCA 866 chrX ENST00000376327.5 PPBP UUGGCGAAAGGCAAAGGUAG 867 chr4 ENST00000296028.3 PPBP GUCAUUGCUGCUGACUGCUC 868 chr4 ENST00000296028.3 PPBP AAGGGGUGGUAUCAAGUCUG 869 chr4 ENST00000296028.3 PXDN ACCACAGUUCAGCUCUUCCG 870 chr2 ENST00000252804.8 PXDN GCGUCUGGGAUAUUCACAGA 871 chr2 ENST00000252804.8 PXDN ACUGCGACUGUGAAAUCCUG 872 chr2 ENST00000252804.8 RORC CCGCGUUACAGCGCUGGCUC 873 chr1 ENST00000318247.6 RORC AGUAGGCCGCGUUACAGCGC 874 chr1 ENST00000318247.6 RORC CUGCUGACGGGUGCAGGAGU 875 chr1 ENST00000318247.6 RORC GCAGUUCUGCUGACGGGUGC 876 chr1 ENST00000318247.6 SCG2 AGCCCUGAUCAUUUCAGGAC 877 chr2 ENST00000305409.2 SCG2 CUGGUUCUUUCUGAAGCAGC 878 chr2 ENST00000305409.2 SCG2 UGGCUGAAGCAAAGACCCAC 879 chr2 ENST00000305409.2 SCGB3A1 CCUCUAUGAGGUGGUUCACG 880 chr5 ENST0000029264L3 SCGB3A1 GGUGCCGAGGGGGUUGGCCA 881 chr5 ENST0000029264L3 SCGB3A1 UGCAGCUGCUGCUUUCUUAG 882 chr5 ENST0000029264L3 SECTM1 ACAGCCCAGCAUGGGAGUCC 883 chr17 ENST00000269389.7 SECTM1 CUGGAGCUGCCAGCCGUCCC 884 chr17 ENST00000269389.7 SECTM1 CUUGAUGUUGACAUGGGAGA 885 chr17 ENST00000269389.7 SLURP1 CCCUGACUCCAGUGCACCCA 886 chr8 ENST00000246515.1 SLURP1 CGUCACCAGCGUGGUCAUGC 887 chr8 ENST00000246515.1 SLURP1 CUUGCAGGUGUAGCACUUGA 888 chr8 ENST00000246515.1 SOSTDC1 AUCAAGCCAGAAAUGGAGGC 889 chr7 ENST00000307068.4 SOSTDC1 AGAAAUCCUUUAUUCACAUG 890 chr7 ENST00000307068.4 SOSTDC1 UUAGGAUGCAUGCAAGGGGA 891 chr7 ENST00000307068.4 SP100 UCUGAGAGUCCAUUUUCAGG 892 chr2 ENST00000340126.8 SP100 AGUGACAAAGAUGAUUCGCU 893 chr2 ENST00000340126.8 SP100 ACCCAGUCAGUCUUACCUGU 894 chr2 ENST00000340126.8 SP11 GUCCCCCACAGACCAUUACU 895 chr11 ENST00000378538.7 SP11 GGGGGUGGAAGUCCCAGUAA 896 chr11 ENST00000378538.7 SP11 CGCUGUGCACGUGGUGGGGG 897 chr11 ENST00000378538.7 SP11 ACUCGCUGUGCACGUGGUGG 898 chr11 ENST00000378538.7 SPP1 AAUGGUGAGACUCAUCAGAC 899 chr4 ENST00000237623.11 SPP1 UCGGUUGCUGGCAGGUCCGU 900 chr4 ENST00000237623.11 SPP1 UGAUGGCCGAGGUGAUAGUG 901 chr4 ENST00000237623.11 TBX21 CCCGCCCCGGAUGGGCAUCG 902 ch17 ENST00000177694.1 TBX21 GGCAUCGUGGAGCCGGGUUG 903 ch17 ENST00000177694.1 TBX21 GGGUUGCGGAGACAUGCUGA 904 ch17 ENST00000177694.1 TBX21 GUCGCUCCCCGGCAUCGGCU 905 ch17 ENST00000177694.1 TCAP GCACUGCCCCUGCUGGUGGU 906 chr17 ENST00000309889.2 TCAP AGUACCAGCUGCCCUACCAG 907 chr17 ENST00000309889.2 TCAP CUCCUUGGUGGCGCCCAUCU 908 chr17 ENST00000309889.2 TGFB1* GCCGCAGCUUGGACAGGAUC 909 chr19 ENST00000221930.5 TGFB1* CUCCAUGUCGAUAGUCUUGC 910 chr19 ENST00000221930.5 TGFB1* AGCAGCCGCAGCCCGGAGGG 911 chr19 ENST00000221930.5 TGFB2* UACCUGCAGCACACUCGAUA 912 chr1 ENST00000366930.8 TGFB2* UCGGGCUCAGGAUAGUCUUC 913 chr1 ENST00000366930.8 TGFB2* CUUCUCCUGGAGCAAGUCCC 914 chr1 ENST00000366930.8 TGFB3* GACAGAUCUUGAGCAAGCUC 915 chr14 ENST00000238682.7 TGFB3* UGGUGCAAGUGGACAGAGAG 916 chr14 ENST00000238682.7 TGFB3* GCACUUGCAAAGGGCUCUGG 917 chr14 ENST00000238682.7 TGFBR1** UUUUCAGUAAAGUCAUCACC 918 chr9 ENST00000374994.8 TGFBR1** CUGCAUCUCACUCAUGUUGA 919 chr9 ENST00000374994.8 TGFBR1** CCUCUUCAUUUGGCACUCGA 920 chr9 ENST00000374994.8 TGFBR2** UCUACUGCUACCGCGUUAAC 921 chr3 ENST00000295754.9 TGFBR2** CGAGCACUGUGCCAUCAUCC 922 chr3 ENST00000295754.9 TGFBR2** GUUGAUGUUGUUGGCACACG 923 chr3 ENST00000295754.9 TGFBR3** CAGCCCAGUUGUGCCUCUGC 924 chr1 ENST00000212355.8 TGFBR3** CAUCAAGGCCUGGACAGGAU 925 chr1 ENST00000212355.8 TGFBR3** CCCUUGGCAGGUCCAGAGCC 926 chr1 ENST00000212355.8 THBS1 UCCUGUCUAACAGAGUCUGG 927 chr15 ENST00000260356.5 THBS1 GUCGGCGCCCAGACCCCUUG 928 chr15 ENST00000260356.5 THBS1 UCAGGUUGGCAUCCUCGAUG 929 chr15 ENST00000260356.5 THNSL2 GAGAAGUGGUCCAUCUGUCC 930 chr2 ENST00000324166.6 THNSL2 UGGCGUCACAUAUGCAUUUA 931 chr2 ENST00000324166.6 THNSL2 UCUUCUCCAGGAAGUACUGC 932 chr2 ENST00000324166.6 THPO CCUGUCCAGAAAGCUGCCCC 933 chr3 ENST00000204615.11 THPO CCAUCACUCCCUCCAGCAGA 934 chr3 ENST00000204615.11 THPO UCUUUCUCAGGAGGAGACCA 935 chr3 ENST00000204615.11 TIMP1 CAGGGGCUCAAAGGGGGCCA 936 chrX ENST00000218388.8 TIMP1 GACACAGGUGCAGGCCCUGC 937 chrX ENST00000218388.8 TIMP1 GGGUGAGGACUCACCGAGGU 938 chrX ENST00000218388.8 TNF* GAUCAUGCUUUCAGUGCUCA 939 chr6 ENST00000449264.2 TNF* CAAGAAGACAGGGGGGCCCC 940 chr6 ENST00000449264.2 TNF* GGCGCCUGCCACGAUCAGGA 941 chr6 ENST00000449264.2 TNFRSF4** CCGGCCCCUGCUCAGGAAGU 942 chr1 ENST00000379236.3 TNFRSF4** UGAGCGGAAGCAGCUGUGCA 943 chr1 ENST00000379236.3 TNFRSF4** GCAGCUGUGCACGGCCACAC 944 chr1 ENST00000379236.3 TNFRSF4** GCGGCAGACUGUGUCCUGUG 945 chr1 ENST00000379236.3 TNFRSF11** GUCUCCCGCAGGCAAGGCCC 946 chr18 ENST00000586569.2 TNFRSF11** CCCCCGGCGCUGCGCGUGCA 947 chr18 ENST00000586569.2 TNFRSF11** CCGCAACACCGAGUGCGCGC 948 chr18 ENST00000586569.2 TNFRSF11** GCCAGCUGUCUGUGUAGUAG 949 chr8 ENST00000297350.8 TNFRSF11** AACAACACUGUACAGCAAAG 950 chr8 ENST00000297350.8 TNFRSF11** ACUUUGGAGGAAACGUUUCC 951 chr8 ENST00000297350.8 TNFRSF1A AGCAAAUCGAAUUAUUUUGA 952 chr12 ENST00000162749.6 TNFRSF1A UUCUCCCUGUCCCCUAGGUG 953 chr12 ENST00000162749.6 TNFRSF1A CCAGGUGCUCCUGGAGCUGU 954 chr12 ENST00000162749.6 TNFRSF9** UGUGAACAGGAUUGUAAACA 955 chr1 ENST00000377507.7 TNFRSF9** CAGAGUGUGACUGCACUCCA 956 chr1 ENST00000377507.7 TNFRSF9** GGGACUUUGUAGGUGUUUUC 957 chr1 ENST00000377507.7 TNFSF9*** GGGGUCCAGUGAAGCGUCAG 958 chr19 ENST00000245817.4 TNFSF9*** AUACGCCUCUGACGCUUCAC 959 chr19 ENST00000245817.4 TNFSF9*** CGGGAGGCCACGGGGCUUCG 960 chr19 ENST00000245817.4 TNFSF9*** CACUGGACCCCGAAGCCCCG 961 chr19 ENST00000245817.4 TNFSF10 CUACCUUUCUAACGAGCUGA 962 chr3 ENST00000241261.6 TNFSF10 GUUCAUACUCUCUUCGUCAU 963 chr3 ENST00000241261.6 TNFSF10 GAAACAAGCAAUGCCACUUU 964 chr3 ENST00000241261.6 TNFSF11 CCAUCUUCUGAUAUUCUAUU 965 chr13 ENST00000398795.6 TNFSF11 AGAUUUUCAAGACACAACUC 966 chr13 ENST00000398795.6 TNFSF11 UUCAUGUAGGAGAAUUAAAC 967 chr13 ENST00000398795.6 TNFSF12 CCGCCCCCAUGGCCGCCCGU 968 chr17 ENST00000293825.10 TNFSF12 CCUGCUGGUCCCGCUCGCGC 969 chr17 ENST00000293825.10 TNFSF12 CCGGGCAUCGCUGUCCGCCC 970 chr17 ENST00000293825.10 TNFSF12- CCGCCCCCAUGGCCGCCCGU 971 chr17 ENST00000293826.4 TNFSF12- CCUGCUGGUCCCGCUCGCGC 972 chr17 ENST00000293826.4 TNFSF12- CCGGGCAUCGCUGUCCGCCC 973 chr17 ENST00000293826.4 TNFSF13 GGGGGGCCCAGUCAGAGAGC 974 chr17 ENST00000338784.8 TNFSF13 CAGAGCCAUGGCACAAGCCA 975 chr17 ENST00000338784.8 TNFSF13 AGAGAGGUGAGCCGGCUGCA 976 chr17 ENST00000338784.8 TNFSF13B UCAUUUCUUCUCUUUUCUUA 977 chr13 ENST00000375887.8 TNFSF13B CUCCAAAGACGGAAAGCUGC 978 chr13 ENST00000375887.8 TNFSF13B CACGGUGGUGUCUUUCUACC 979 chr13 ENST00000375887.8 TNFSF14 CACACCGCCCAGCUGCACCU 980 chr19 ENST00000599359.1 TNFSF14 GGGCCCCAUCGUGGUAGCUG 981 chr19 ENST00000599359.1 TNFSF14 GCUGCCGGUCAAGCUGGAGU 982 chr19 ENST00000599359.1 TNFSF15 UCAUCCCACGGAAUGUGACC 983 chr9 ENST00000374045.4 TNFSF15 AUUUGUUGGUAUAGUUCAUU 984 chr9 ENST00000374045.4 TNFSF15 UGAUUUUUAAAGUGCUGUGU 985 chr9 ENST00000374045.4 TNFSF18 AAUAAAGAUUAGCCAACUGA 986 chr1 ENST00000404377.3 TNFSF18 GCAAAAGAGCCACAGCUUCC 987 chr1 ENST00000404377.3 TNFSF18 AAGUGGCUCAAACACAUUUU 988 chr1 ENST00000404377.3 TNFSF4 CCUCAUCCUUCUGGUAAUGA 989 chr1 ENST00000281834.3 TNFSF4 GUUUUAUCUCAUCUCCCUGA 990 chr1 ENST00000281834.3 TNFSF4 CUAGAAUAUAAGAAGGAGAA 991 chr1 ENST00000281834.3 TNFSF8 UCUGUGCCUUGUCUUCACGG 992 chr9 ENST00000223795.2 TNFSF8 GCUCGUGGUCCCCAGGUGGC 993 chr9 ENST00000223795.2 TNFSF8 UGAGUGCUUGCUGCAGCCCU 994 chr9 ENST00000223795.2 TNFSF9 AUACGCCUCUGACGCUUCAC 995 chr19 ENST00000245817.4 TNFSF9 ACGCGGCAGGCGCGAGCGCG 996 chr19 ENST00000245817.4 TNFSF9 CGUCUUCCUCGCCUGCCCCU 997 chr19 ENST00000245817.4 TRIM16 CUCCUCGGAGAAGCUUGGCA 998 chr17 ENST00000336708.11 TRIM16 GGUCACCCAGCCCAGAUUCU 999 chr17 ENST00000336708.11 TRIM16 AGCCUCCCAGAUGGCUGAGU 1000 chr17 ENST00000336708.11 TSLP UGGAUUUCAGUAAGGCAAUG 1001 chr5 ENST00000344895.3 TSLP AAUGUUCGCCAUGAAAACUA 1002 chr5 ENST00000344895.3 TSLP CAAGGUACAGCAAACGUCUG 1003 chr5 ENST00000344895.3 TWSG1 GUGAGUGCCCGGAAGAGAGA 1004 chr18 ENST00000262120.9 TWSG1 UGUGAAAGUUCUUCUGCAAC 1005 chr18 ENST00000262120.9 TWSG1 ACAGACACAUUCUGGUGGUG 1006 chr18 ENST00000262120.9 TXLNA UAACCAGGGGGGCCCCGGCG 1007 chr1 ENST00000373609.1 TXLNA AGAGAAGUCCCGGACCUAUG 1008 chr1 ENST00000373609.1 TXLNA UGUGUUUGGAUCCCCCUUGG 1009 chr1 ENST00000373609.1 VASN GGCAGCUUUGCCGGCCUGCC 1010 chr16 ENST00000304735.3 VASN ACUCGCCAACCUCAGCAACC 1011 chr16 ENST00000304735.3 VASN AUGAGACCUUCCGUGGCCUG 1012 chr16 ENST00000304735.3 VEGFA CAGGGGCCGGAGCCCGCGCC 1013 chr6 ENST00000425836.6 VEGFA UUCUCGCUUCGGAGGAGCCG 1014 chr6 ENST00000425836.6 VEGFA AAGUGCUAGCUCGGGCCGGG 1015 chr6 ENST00000425836.6 VSTM1 CGAAGCUGAAUUCCCCUUCA 1016 chr19 ENST00000338372.6 VSTM1 UGCGCAAGGUGAACGACUCU 1017 chr19 ENST00000338372.6 VSTM1 UUCAACCACCGAGCUGGGCC 1018 chr19 ENST00000338372.6 WFIKKN1 GCUCCUUCUCACAGCGGUCG 1019 chr16 ENST00000319070.2 WFIKKN1 CCGCUGCUAUAUGGACGCCG 1020 chr16 ENST00000319070.2 WFIKKN1 CCUGCAAGCACGUGCUCAGC 1021 chr16 ENST00000319070.2 WFIKKN2 GUGCAAAGACCGCUGUGAGA 1022 chr17 ENST00000311378.4 WFIKKN2 CCGCUGCUACAUGGAUGCCG 1023 chr17 ENST00000311378.4 WFIKKN2 CCUGCCGCUAUCACUUCACC 1024 chr17 ENST00000311378.4 WNT1 AGACUCCAAGAGUCUGCAAC 1025 chr12 ENST00000293549.3 WNT1 GCGUCUGAUACGCCAAAAUC 1026 chr12 ENST00000293549.3 WNT1 GGCAGUUCCGGAAUCGCCGC 1027 chr12 ENST00000293549.3 WNT2 UGUUGCAAUUCCAGCGGUGC 1028 chr7 ENST00000265441.7 WNT2 CUAAUGGCACGCAUCACAUC 1029 chr7 ENST00000265441.7 WNT2 GAGCUACAGGUGGCUCCUCC 1030 chr7 ENST00000265441.7 WNT5A UGCAGUUCCACCUUCGAUGU 1031 chr3 ENST00000264634.8 WNT5A CUUCUCCGAUGUACUGCAUG 1032 chr3 ENST00000264634.8 WNT5A CCUGCCAGUUGGCUGCAGAG 1033 chr3 ENST00000264634.8 WNT7A AGAGCGCACCGUCUUCGGGA 1034 chr3 ENST00000285018.4 WNT7A ACUGAAACUGACACUCGUCC 1035 chr3 ENST00000285018.4 WNT7A UGGCAGAUCGCCCGCUGUCU 1036 chr3 ENST00000285018.4 XCL1* GGAGUGAAGUCUCAGAUAAG 1037 chr1 ENST00000367818.3 XCL1* GGAGUGAAGUCUCAGAUAAG 1038 chr1 ENST00000367818.3 XCL1* GGAGUGAAGUCUCAGAUAAG 1039 chr1 ENST00000367818.3 XCL2* GAGUGUAUUUCUAUACCUCU 1040 chr1 ENST00000367819.2 XCL2* UAGGGAGUGAAGUCUCACAU 1041 chr1 ENST00000367819.2 XCL2* UAGGGAGUGAAGUCUCACAU 1042 chr1 ENST00000367819.2 ZFP36 CCUCCAUGGUCGGAUGGCAC 1043 chr19 ENST00000597629.1 ZFP36 UCGGAGGGGCUCAGGCUCCA 1044 chr19 ENST00000597629.1 ZFP36 GGAGGGCCGCAGCUGUGGCU 1045 chr19 ENST00000597629.1 *indicates cytokines/chemokines produced by T cells that activate or localize myeloid cells **indicates T cell surface receptor genes that activate myeloid or CAR-T cells ***indicates T cell surface receptors that arc integrated into CAR-T cell signaling thus endogenous receptors are redundant {circumflex over ( )}indicates cytokines that drive T cell/CAR-T cell differentiation Bold rows indicate transcription factors that drive T cell/CAR-T cell differentiation

Example 6—Protocol—Nucleofection Using Nucleofector 4D

4×10⁶ cells per reaction are used. EO-115-100 μl transfection volume is programmed, and the entire supplement added to the Nucleofector™ Solution P3. Cell culture plates are prepared by filling appropriate number of wells with desired volume of recommended culture media (2 ml in 6 well plate) and pre-incubating/equilibrating plates in a humidified 37° C./5% CO₂ incubator. Beads are magnetically removed (twice to ensure complete removal), then cells counted and cell density determined. The required number of cells are centrifuged at 90×g for 10 minutes at room temperature, the supernatant removed completely. Cells are then resuspended in PBS (1 ml) and transferred to a microcentrifuge tube, and the required number of cells centrifuged at 90×g for 10 minutes at room temperature. The supernatant is removed completely, and the cell pellet resuspended carefully in complete room temperature 4D Nucleofector™ Solution P3, 4×10⁶ per 100 μl). Twenty μg of gRNA (gGM-CSF) is added to each tube of 15 μg Cas9 mRNA. Then 100 μl of cells is added to each tube of Cas9/gRNA, gently mixed and everything transferred into the Nucleocuvette™. The cuvette is gently tapped to remove bubbles. Electroporation is carried out using program (Human T cell stim EO-115). After run completion, the Nucleocuvette™ is carefully removed from the vessel from the retainer using a specialized tool. Cells are resuspended with pre-warmed medium. The media is then taken up from destination well, added to cuvette, and gently pipetted up and down two to three times. This is then transferred to well. This procedure is repeated with media from same well and incubated at 37° C.

CAR Transduction (Day 2).

Genome-edited CAR-T cells may then be transduced with one or more CARs targeted to (i.e., that recognizes) one or more targets, for example with a lentivirus containing a CAR construct. Any other suitable method of transduction may be used.

Protocol—To transduce T cells with lentivirus: One μl of polybrene is added for each ml media (8 mg/ml stock). The required amount of virus is then added to give required M.O.I. Cells and virus are mixed and placed back in incubator at 37° C.

Assessment of Transduction Efficiency (Day 10).

Samples of cells may then be assessed for transduction efficiency by taking a 5×10⁵ cells from each sample and analyzing by flow cytometry. Samples are washed with RB, and 3 μl of anti-CD34 PE antibody added (to detect the CAR as the construct contains human truncated CD34). Thereafter, 5 ul of CD3 APC is added, the cells washed, and flow cytometry performed. CAR-T cells should be CD3ε positive, CD34 positive.

Assessment of Genetic Deletion.

To assess genetic deletion, 5×10⁵ cells are harvested from each sample and their DNA extracted. Gene editing efficiency is assessed using target sequencing of the target loci using TIDE-analysis or deep sequencing.

Assessment of tumor burden and cytokine level.

T cells are harvested (Day 11). Tumor burden may be imaged in mouse using bioluminescent imaging. 3×10⁷ CAR-T are injected per mouse I.P.

Serum cytokine levels (Day 12) are measured, e.g., using the Luminex multiplex cytokine profiling assay to check for elevations in CRS-related cytokines. A 4-hr chromium release assay against targets cells (Raji) may be performed to assess in vitro activity (Day 11).

Example 7—Additional Examples of CAR-Bearing Immune Effector Cells

Several types of chimeric antigen receptor (CAR)-bearing immune effector cells that are deficient in a cytokine may be made using the methods above. Tables 11-13 below give Examples.

TABLE 11 Mono, TCR Gene Dual, or CAR Antigen Modifica- Deleted/ Example Cell Tandem Target(s) Deletion(s) tions Suppressed 1 T-Cell Mono CD19 — — GM-CSF 2 T-Cell Mono CD19 — — CCL2 3 T-Cell Mono CD19 — — MCP-2 4 T-Cell Mono CD19 — — G-CSF 5 T-Cell Mono CD19 — — M-CSF 6 T-Cell Mono CD19 — — Il-4 7 T-Cell Mono CD19 — — IFNγ 8 T-Cell Mono CD19 — TRAC GM-CSF 9 T-Cell Mono CD19 — TRAC CCL2 10 T-Cell Mono CD19 — TRAC MCP-2 11 T-Cell Mono CD19 — TRAC G-CSF 12 T-Cell Mono CD19 — TRAC M-CSF 13 T-Cell Mono CD19 — TRAC Il-4 14 T-Cell Mono CD19 — TRAC IFNγ 15 T-Cell Mono CD20 — — GM-CSF 16 T-Cell Mono CD20 — — CCL2 17 T-Cell Mono CD20 — — MCP-2 18 T-Cell Mono CD20 — — G-CSF 19 T-Cell Mono CD20 — — M-CSF 20 T-Cell Mono CD20 — — Il-4 21 T-Cell Mono CD20 — — IFNγ 22 T-Cell Mono CD20 — TRAC GM-CSF 23 T-Cell Mono CD20 — TRAC CCL2 24 T-Cell Mono CD20 — TRAC MCP-2 25 T-Cell Mono CD20 — TRAC G-CSF 26 T-Cell Mono CD20 — TRAC M-CSF 27 T-Cell Mono CD20 — TRAC Il-4 28 T-Cell Mono CD20 — TRAC IFNγ 29 T-Cell Mono BCMA — — GM-CSF 30 T-Cell Mono BCMA — — CCL2 31 T-Cell Mono BCMA — — MCP-2 32 T-Cell Mono BCMA — — G-CSF 33 T-Cell Mono BCMA — — M-CSF 34 T-Cell Mono BCMA — — Il-4 35 T-Cell Mono BCMA — — IFNγ 36 T-Cell Mono BCMA — TRAC GM-CSF 37 T-Cell Mono BCMA — TRAC CCL2 38 T-Cell Mono BCMA — TRAC MCP-2 39 T-Cell Mono BCMA — TRAC G-CSF 40 T-Cell Mono BCMA — TRAC M-CSF 41 T-Cell Mono BCMA — TRAC Il-4 42 T-Cell Mono BCMA — TRAC IFNγ 43 T-Cell Mono Mesothelin — — GM-CSF 44 T-Cell Mono Mesothelin — — CCL2 45 T-Cell Mono Mesothelin — — MCP-2 46 T-Cell Mono Mesothelin — — G-CSF 47 T-Cell Mono Mesothelin — — M-CSF 48 T-Cell Mono Mesothelin — — Il-4 49 T-Cell Mono Mesothelin — — IFNγ 50 T-Cell Mono Mesothelin — TRAC GM-CSF 51 T-Cell Mono Mesothelin — TRAC CCL2 52 T-Cell Mono Mesothelin — TRAC MCP-2 53 T-Cell Mono Mesothelin — TRAC G-CSF 54 T-Cell Mono Mesothelin — TRAC M-CSF 55 T-Cell Mono Mesothelin — TRAC Il-4 56 T-Cell Mono Mesothelin — TRAC IFNγ 57 T-Cell Mono CD7 CD7 TRAC GM-CSF 58 T-Cell Mono CD7 CD7 TRAC CCL2 59 T-Cell Mono CD7 CD7 TRAC MCP-2 60 T-Cell Mono CD7 CD7 TRAC G-CSF 61 T-Cell Mono CD7 CD7 TRAC M-CSF 62 T-Cell Mono CD7 CD7 TRAC Il-4 63 T-Cell Mono CD7 CD7 TRAC IFNγ 64 T-Cell Mono CD3ε CD3ε — GM-CSF 65 T-Cell Mono CD3ε CD3ε — CCL2 66 T-Cell Mono CD3ε CD3ε — MCP-2 67 T-Cell Mono CD3ε CD3ε — G-CSF 68 T-Cell Mono CD3ε CD3ε — M-CSF 69 T-Cell Mono CD3ε CD3ε — Il-4 70 T-Cell Mono CD3ε CD3ε — IFNγ 71 T-Cell Mono CD2 CD2 TRAC GM-CSF 72 T-Cell Mono CD2 CD2 TRAC CCL2 73 T-Cell Mono CD2 CD2 TRAC MCP-2 74 T-Cell Mono CD2 CD2 TRAC G-CSF 75 T-Cell Mono CD2 CD2 TRAC M-CSF 76 T-Cell Mono CD2 CD2 TRAC Il-4 77 T-Cell Mono CD2 CD2 TRAC IFNγ 78 T-Cell Mono CD5 — TRAC GM-CSF 79 T-Cell Mono CD5 — TRAC CCL2 80 T-Cell Mono CD5 — TRAC MCP-2 81 T-Cell Mono CD5 — TRAC G-CSF 82 T-Cell Mono CD5 — TRAC M-CSF 83 T-Cell Mono CD5 — TRAC Il-4 84 T-Cell Mono CD5 — TRAC IFNγ 85 T-Cell Mono CD5 CD5 TRAC GM-CSF 86 T-Cell Mono CD5 CD5 TRAC CCL2 87 T-Cell Mono CD5 CD5 TRAC MCP-2 88 T-Cell Mono CD5 CD5 TRAC G-CSF 89 T-Cell Mono CD5 CD5 TRAC M-CSF 90 T-Cell Mono CD5 CD5 TRAC Il-4 91 T-Cell Mono CD5 CD5 TRAC IFNγ 92 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC GM-CSF 93 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC CCL2 94 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC MCP-2 95 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC G-CSF 96 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC M-CSF 97 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC Il-4 98 T-Cell Tandem CD7 × CD2 CD7 & CD2 TRAC IFNγ 99 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — GM-CSF 100 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — CCL2 101 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — MCP-2 102 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — G-CSF 103 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — M-CSF 104 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — Il-4 105 T-Cell Tandem CD3ε × CD2 CD3 & CD2 — IFNγ 106 T-Cell Tandem CD19 × CD20 — TRAC GM-CSF 107 T-Cell Tandem CD19 × CD20 — TRAC CCL2 108 T-Cell Tandem CD19 × CD20 — TRAC MCP-2 109 T-Cell Tandem CD19 × CD20 — TRAC G-CSF 110 T-Cell Tandem CD19 × CD20 — TRAC M-CSF 111 T-Cell Tandem CD19 × CD20 — TRAC Il-4 112 T-Cell Tandem CD19 × CD20 — TRAC IFNγ 113 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC GM-CSF 114 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC CCL2 115 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC MCP-2 116 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC G-CSF 117 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC M-CSF 118 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC Il-4 119 T-Cell Dual CD7 × CD2 CD7 & CD2 TRAC IFNγ 120 T-Cell Dual CD3ε × CD2 CD3 & CD2 — GM-CSF 121 T-Cell Dual CD3ε × CD2 CD3 & CD2 — CCL2 122 T-Cell Dual CD3ε × CD2 CD3 & CD2 — MCP-2 123 T-Cell Dual CD3ε × CD2 CD3 & CD2 — G-CSF 124 T-Cell Dual CD3ε × CD2 CD3 & CD2 — M-CSF 125 T-Cell Dual CD3ε × CD2 CD3 & CD2 — Il-4 126 T-Cell Dual CD3ε × CD2 CD3 & CD2 — IFNγ 127 T-Cell Dual CD19 × CD20 — TRAC GM-CSF 128 T-Cell Dual CD19 × CD20 — TRAC CCL2 129 T-Cell Dual CD19 × CD20 — TRAC MCP-2 130 T-Cell Dual CD19 × CD20 — TRAC G-CSF 131 T-Cell Dual CD19 × CD20 — TRAC M-CSF 132 T-Cell Dual CD19 × CD20 — TRAC Il-4 133 T-Cell Dual CD19 × CD20 — TRAC IFNγ

TABLE 12 Mono, Gene Dual, or CAR Antigen Deleted/ Example Cell Tandem Target(s) Deletion(s) Suppressed 134 NK Cell Mono CD19 — GM-CSF 135 NK Cell Mono CD19 — CCL2 136 NK Cell Mono CD19 — MCP-2 137 NK Cell Mono CD19 — G-CSF 138 NK Cell Mono CD19 — M-CSF 139 NK Cell Mono CD19 — Il-4 140 NK Cell Mono CD19 — IFNγ 141 NK Cell Mono CD19 — GM-CSF 142 NK Cell Mono CD19 — CCL2 143 NK Cell Mono CD19 — MCP-2 144 NK Cell Mono CD19 — G-CSF 145 NK Cell Mono CD19 — M-CSF 146 NK Cell Mono CD19 — Il-4 147 NK Cell Mono CD19 — IFNγ 148 NK Cell Mono CD20 — GM-CSF 149 NK Cell Mono CD20 — CCL2 150 NK Cell Mono CD20 — MCP-2 151 NK Cell Mono CD20 — G-CSF 152 NK Cell Mono CD20 — M-CSF 153 NK Cell Mono CD20 — Il-4 154 NK Cell Mono CD20 — IFNγ 155 NK Cell Mono CD20 — GM-CSF 156 NK Cell Mono CD20 — CCL2 157 NK Cell Mono CD20 — MCP-2 158 NK Cell Mono CD20 — G-CSF 159 NK Cell Mono CD20 — M-CSF 160 NK Cell Mono CD20 — Il-4 161 NK Cell Mono CD20 — IFNγ 162 NK Cell Mono BCMA — GM-CSF 163 NK Cell Mono BCMA — CCL2 164 NK Cell Mono BCMA — MCP-2 165 NK Cell Mono BCMA — G-CSF 166 NK Cell Mono BCMA — M-CSF 167 NK Cell Mono BCMA — Il-4 168 NK Cell Mono BCMA — IFNγ 169 NK Cell Mono BCMA — GM-CSF 170 NK Cell Mono BCMA — CCL2 171 NK Cell Mono BCMA — MCP-2 172 NK Cell Mono BCMA — G-CSF 173 NK Cell Mono BCMA — M-CSF 174 NK Cell Mono BCMA — Il-4 175 NK Cell Mono BCMA — IFNγ 176 NK Cell Mono Mesothelin — GM-CSF 177 NK Cell Mono Mesothelin — CCL2 178 NK Cell Mono Mesothelin — MCP-2 179 NK Cell Mono Mesothelin — G-CSF 180 NK Cell Mono Mesothelin — M-CSF 181 NK Cell Mono Mesothelin — Il-4 182 NK Cell Mono Mesothelin — IFNγ 183 NK Cell Mono Mesothelin — GM-CSF 184 NK Cell Mono Mesothelin — CCL2 185 NK Cell Mono Mesothelin — MCP-2 186 NK Cell Mono Mesothelin — G-CSF 187 NK Cell Mono Mesothelin — M-CSF 188 NK Cell Mono Mesothelin — Il-4 189 NK Cell Mono Mesothelin — IFNγ 190 NK Cell Mono CD7 CD7 GM-CSF 191 NK Cell Mono CD7 CD7 CCL2 192 NK Cell Mono CD7 CD7 MCP-2 193 NK Cell Mono CD7 CD7 G-CSF 194 NK Cell Mono CD7 CD7 M-CSF 195 NK Cell Mono CD7 CD7 Il-4 196 NK Cell Mono CD7 CD7 IFNγ 197 NK Cell Mono CD3ε CD3ε GM-CSF 198 NK Cell Mono CD3ε CD3ε CCL2 199 NK Cell Mono CD3ε CD3ε MCP-2 200 NK Cell Mono CD3ε CD3ε G-CSF 201 NK Cell Mono CD3ε CD3ε M-CSF 202 NK Cell Mono CD3ε CD3ε Il-4 203 NK Cell Mono CD3ε CD3ε IFNγ 204 NK Cell Mono CD2 CD2 GM-CSF 205 NK Cell Mono CD2 CD2 CCL2 206 NK Cell Mono CD2 CD2 MCP-2 207 NK Cell Mono CD2 CD2 G-CSF 208 NK Cell Mono CD2 CD2 M-CSF 209 NK Cell Mono CD2 CD2 Il-4 210 NK Cell Mono CD2 CD2 IFNγ 211 NK Cell Mono CD5 — GM-CSF 212 NK Cell Mono CD5 — CCL2 213 NK Cell Mono CD5 — MCP-2 214 NK Cell Mono CD5 — G-CSF 215 NK Cell Mono CD5 — M-CSF 216 NK Cell Mono CD5 — Il-4 217 NK Cell Mono CD5 — IFNγ 218 NK Cell Tandem CD7xCD2 CD7 & CD2 GM-CSF 219 NK Cell Tandem CD7xCD2 CD7 & CD2 CCL2 220 NK Cell Tandem CD7xCD2 CD7 & CD2 MCP-2 221 NK Cell Tandem CD7xCD2 CD7 & CD2 G-CSF 222 NK Cell Tandem CD7xCD2 CD7 & CD2 M-CSF 223 NK Cell Tandem CD7xCD2 CD7 & CD2 Il-4 224 NK Cell Tandem CD7xCD2 CD7 & CD2 IFNγ 225 NK Cell Tandem CD3εxCD2 CD3 & CD2 GM-CSF 226 NK Cell Tandem CD3εxCD2 CD3 & CD2 CCL2 227 NK Cell Tandem CD3εxCD2 CD3 & CD2 MCP-2 228 NK Cell Tandem CD3εxCD2 CD3 & CD2 G-CSF 229 NK Cell Tandem CD3εxCD2 CD3 & CD2 M-CSF 230 NK Cell Tandem CD3εxCD2 CD3 & CD2 Il-4 231 NK Cell Tandem CD3εxCD2 CD3 & CD2 IFNγ 232 NK Cell Tandem CD19xCD20 — GM-CSF 233 NK Cell Tandem CD19xCD20 — CCL2 234 NK Cell Tandem CD19xCD20 — MCP-2 235 NK Cell Tandem CD19xCD20 — G-CSF 236 NK Cell Tandem CD19xCD20 — M-CSF 237 NK Cell Tandem CD19xCD20 — Il-4 238 NK Cell Tandem CD19xCD20 — IFNγ 239 NK Cell Dual CD7xCD2 CD7 & CD2 GM-CSF 240 NK Cell Dual CD7xCD2 CD7 & CD2 CCL2 241 NK Cell Dual CD7xCD2 CD7 & CD2 MCP-2 242 NK Cell Dual CD7xCD2 CD7 & CD2 G-CSF 243 NK Cell Dual CD7xCD2 CD7 & CD2 M-CSF 244 NK Cell Dual CD7xCD2 CD7 & CD2 Il-4 245 NK Cell Dual CD7xCD2 CD7 & CD2 IFNγ 246 NK Cell Dual CD3εxCD2 CD3 & CD2 GM-CSF 247 NK Cell Dual CD3εxCD2 CD3 & CD2 CCL2 248 NK Cell Dual CD3εxCD2 CD3 & CD2 MCP-2 249 NK Cell Dual CD3εxCD2 CD3 & CD2 G-CSF 250 NK Cell Dual CD3εxCD2 CD3 & CD2 M-CSF 251 NK Cell Dual CD3εxCD2 CD3 & CD2 Il-4 252 NK Cell Dual CD3εxCD2 CD3 & CD2 IFNγ 253 NK Cell Dual CD19xCD20 — GM-CSF 254 NK Cell Dual CD19xCD20 — CCL2 255 NK Cell Dual CD19xCD20 — MCP-2 256 NK Cell Dual CD19xCD20 — G-CSF 257 NK Cell Dual CD19xCD20 — M-CSF 258 NK Cell Dual CD19xCD20 — Il-4 259 NK Cell Dual CD19xCD20 — IFNγ

TABLE 13 Mono, Gene Dual, or CAR Antigen Deleted/ Example Cell Tandem Target(s) Deletion(s) Suppressed 260 iNKT Mono CD19 — GM-CSF 261 iNKT Mono CD19 — CCL2 262 iNKT Mono CD19 — MCP-2 263 iNKT Mono CD19 — G-CSF 264 iNKT Mono CD19 — M-CSF 265 iNKT Mono CD19 — Il-4 266 iNKT Mono CD19 — IFNγ 267 iNKT Mono CD19 — GM-CSF 268 iNKT Mono CD19 — CCL2 269 iNKT Mono CD19 — MCP-2 270 iNKT Mono CD19 — G-CSF 271 iNKT Mono CD19 — M-CSF 272 iNKT Mono CD19 — Il-4 273 iNKT Mono CD19 — IFNγ 274 iNKT Mono CD20 — GM-CSF 275 iNKT Mono CD20 — CCL2 276 iNKT Mono CD20 — MCP-2 277 iNKT Mono CD20 — G-CSF 278 iNKT Mono CD20 — M-CSF 279 iNKT Mono CD20 — Il-4 280 iNKT Mono CD20 — IFNγ 281 iNKT Mono CD20 — GM-CSF 282 iNKT Mono CD20 — CCL2 283 iNKT Mono CD20 — MCP-2 284 iNKT Mono CD20 — G-CSF 285 iNKT Mono CD20 — M-CSF 286 iNKT Mono CD20 — Il-4 287 iNKT Mono CD20 — IFNγ 288 iNKT Mono BCMA — GM-CSF 289 iNKT Mono BCMA — CCL2 290 iNKT Mono BCMA — MCP-2 291 iNKT Mono BCMA — G-CSF 292 iNKT Mono BCMA — M-CSF 293 iNKT Mono BCMA — Il-4 294 iNKT Mono BCMA — IFNγ 295 iNKT Mono BCMA — GM-CSF 296 iNKT Mono BCMA — CCL2 297 iNKT Mono BCMA — MCP-2 298 iNKT Mono BCMA — G-CSF 299 iNKT Mono BCMA — M-CSF 300 iNKT Mono BCMA — Il-4 301 iNKT Mono BCMA — IFNγ 302 iNKT Mono Mesothelin — GM-CSF 303 iNKT Mono Mesothelin — CCL2 304 iNKT Mono Mesothelin — MCP-2 305 iNKT Mono Mesothelin — G-CSF 306 iNKT Mono Mesothelin — M-CSF 307 iNKT Mono Mesothelin — Il-4 308 iNKT Mono Mesothelin — IFNγ 309 iNKT Mono Mesothelin — GM-CSF 310 iNKT Mono Mesothelin — CCL2 311 iNKT Mono Mesothelin — MCP-2 312 iNKT Mono Mesothelin — G-CSF 313 iNKT Mono Mesothelin — M-CSF 314 iNKT Mono Mesothelin — Il-4 315 iNKT Mono Mesothelin — IFNγ 316 iNKT Mono CD7 CD7 GM-CSF 317 iNKT Mono CD7 CD7 CCL2 318 iNKT Mono CD7 CD7 MCP-2 319 iNKT Mono CD7 CD7 G-CSF 320 iNKT Mono CD7 CD7 M-CSF 321 iNKT Mono CD7 CD7 Il-4 322 iNKT Mono CD7 CD7 IFNγ 323 iNKT Mono CD3ε CD3ε GM-CSF 324 iNKT Mono CD3ε CD3ε CCL2 325 iNKT Mono CD3ε CD3ε MCP-2 326 iNKT Mono CD3ε CD3ε G-CSF 327 iNKT Mono CD3ε CDε M-CSF 328 iNKT Mono CD3ε CD3ε Il-4 329 iNKT Mono CD3ε CD3ε IFNγ 330 iNKT Mono CD2 CD2 GM-CSF 331 iNKT Mono CD2 CD2 CCL2 332 iNKT Mono CD2 CD2 MCP-2 333 iNKT Mono CD2 CD2 G-CSF 334 iNKT Mono CD2 CD2 M-CSF 335 iNKT Mono CD2 CD2 Il-4 336 iNKT Mono CD2 CD2 IFNγ 337 iNKT Mono CD5 — GM-CSF 338 iNKT Mono CD5 — CCL2 339 iNKT Mono CD5 — MCP-2 340 iNKT Mono CD5 — G-CSF 341 iNKT Mono CD5 — M-CSF 342 iNKT Mono CD5 — Il-4 343 iNKT Mono CD5 — IFNγ 344 iNKT Mono CD5 CD5 GM-CSF 345 iNKT Mono CD5 CD5 CCL2 346 iNKT Mono CD5 CD5 MCP-2 347 iNKT Mono CD5 CD5 G-CSF 348 iNKT Mono CD5 CD5 M-CSF 349 iNKT Mono CD5 CD5 Il-4 350 iNKT Mono CD5 CD5 IFNγ 351 iNKT Tandem CD7xCD2 CD7 & CD2 GM-CSF 352 iNKT Tandem CD7xCD2 CD7 & CD2 CCL2 353 iNKT Tandem CD7xCD2 CD7 & CD2 MCP-2 354 iNKT Tandem CD7xCD2 CD7 & CD2 G-CSF 355 iNKT Tandem CD7xCD2 CD7 & CD2 M-CSF 356 iNKT Tandem CD7xCD2 CD7 & CD2 Il-4 357 iNKT Tandem CD7xCD2 CD7 & CD2 IFNγ 358 iNKT Tandem CD3εxCD2 CD3 & CD2 GM-CSF 359 iNKT Tandem CD3εxCD2 CD3 & CD2 CCL2 360 iNKT Tandem CD3εxCD2 CD3 & CD2 MCP-2 361 iNKT Tandem CD3εxCD2 CD3 & CD2 G-CSF 362 iNKT Tandem CD3εxCD2 CD3 & CD2 M-CSF 363 iNKT Tandem CD3εxCD2 CD3 & CD2 Il-4 364 iNKT Tandem CD3εxCD2 CD3 & CD2 IFNγ 365 iNKT Tandem CD19xCD20 — GM-CSF 366 iNKT Tandem CD19xCD20 — CCL2 367 iNKT Tandem CD19xCD20 — MCP-2 368 iNKT Tandem CD19xCD20 — G-CSF 369 iNKT Tandem CD19xCD20 — M-CSF 370 iNKT Tandem CD19xCD20 — Il-4 371 iNKT Tandem CD19xCD20 — IFNγ 372 iNKT Dual CD7xCD2 CD7 & CD2 GM-CSF 373 iNKT Dual CD7xCD2 CD7 & CD2 CCL2 374 iNKT Dual CD7xCD2 CD7 & CD2 MCP-2 375 iNKT Dual CD7xCD2 CD7 & CD2 G-CSF 376 iNKT Dual CD7xCD2 CD7 & CD2 M-CSF 377 iNKT Dual CD7xCD2 CD7 & CD2 Il-4 378 iNKT Dual CD7xCD2 CD7 & CD2 IFNγ 379 iNKT Dual CD3εxCD2 CD3 & CD2 GM-CSF 380 iNKT Dual CD3εxCD2 CD3 & CD2 CCL2 381 iNKT Dual CD3εxCD2 CD3 & CD2 MCP-2 382 iNKT Dual CD3εxCD2 CD3 & CD2 G-CSF 383 iNKT Dual CD3εxCD2 CD3 & CD2 M-CSF 384 iNKT Dual CD3εxCD2 CD3 & CD2 Il-4 385 iNKT Dual CD3εxCD2 CD3 & CD2 IFNγ 386 iNKT Dual CD19xCD20 — GM-CSF 387 iNKT Dual CD19xCD20 — CCL2 388 iNKT Dual CD19xCD20 — MCP-2 389 iNKT Dual CD19xCD20 — G-CSF 390 iNKT Dual CD19xCD20 — M-CSF 391 iNKT Dual CD19xCD20 — Il-4 392 iNKT Dual CD19xCD20 — IFNγ

Example 8—Biological Assays

The following assays, or variations thereon, may be used to assess efficacy of the cytokine-deficient chimeric antigen receptor (CAR)-bearing immune effector cells disclosed herein.

T-ALL. Testing efficacy of cells in a xenogeneic model of T-ALL: 1×10⁵ Click Beetle Red luciferase (CBR) labeled CCRF-CEM T-ALL (99% CD7+ by FACS) cells will be injected I.V. into NSG recipients prior to infusion of 2×10⁶ to 1×10⁷ CAR7-bearing immune effector cells or non-targeting CAR19-bearing immune effector cells control cells i.v. on day +4. In contrast to mice receiving CART19-bearing immune effector cells or mice injected with tumor only, mice receiving CAR7-bearing immune effector cells will demonstrate significantly prolonged survival and reduced tumor burden as determined by bioluminescent imaging.

Multiple Myeloma. Testing efficacy of iNKT-CAR-CS1 in a xenogeneic model of multiple myeloma: 5×10⁵ Click Beetle Red luciferase (CBR) labeled MM.1S (99% CS1+ by FACS) cells will be injected I.V. into NSG recipients prior to infusion of 2×10⁶ to 1×10⁷ iNKT-CAR-CS1 or non-targeting iNKT-CAR19 control cells i.v. on day +4, or +14 or +28. In contrast to mice receiving iNKT-CAR19 or mice injected with tumor only, mice receiving iNKT-CAR-CS1 will demonstrate significantly prolonged survival and reduced tumor burden as determined by bioluminescent imaging.

In Vivo Models of Cytokine Release Syndrome and Neurotoxicity.

An in vivo mouse model of CRS is disclosed in Giavridis et al., “CAR T cell-induced cytokine release syndrome is mediated by macrophages and abated by IL-1 blockade,” Nat Med 2018 May 28. For example, in order to initiate CRS as a model system, tumor cells are injected intraperitoneally into immune deficient mice and allowed to develop into a tumor. The mice are then given CAR-T cells targeting the cancerous cells and monitored for several days to induce the onset of CRS, after which mice are sacrificed and cells and tissue obtained for analysis. Mice may also be treated for CRS and monitored for success or failure of treatment (i.e., administering antibodies against cytokines produces as a result of administration of CAR-T cells).

Analyses appropriate for monitoring CRS in such a model may include monitoring of weight change in the mice after administration of CAR-T cells, percent survival of mice, serum levels of inflammatory factors, i.e., murine SAA3 (equivalent to human C-reactive protein), cytokine levels before and after administration of CAR-T cells, species of origin of pro-inflammatory cytokines (i.e., human versus murine cytokines; and/or percent survival of mice treated with CAR-T cells that received antibodies against specific cytokines.

Mice that eventually die from CRS symptoms or complications may be classified as having severe CRS, while mice that survive but suffer greater than 10% weight loss may be classified as having non-severe CRS. Using this model, it was discovered that monocytes and macrophages are the main source for IL-6 in CRS.

Another model useful for assessing both CRS and CAR-T associated neuropathy is disclosed in Norelli, “Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells,” Nat Med 2018 May 28. In this model, human stem cells, such as hematopoietic stem and progenitor cells (HSPCs), are injected into humanized NSG mice, which are immunocompromised transgenic mice expressing human stem cell factor, GM-CSF, and IL-3 to support and enhance hematopoiesis from the injected human stem cells. The mice are given tumor cells to serve as targets for subsequently administered CAR-T cells, and then monitored for CRS symptoms. Following injection of CAR-T cells, these mice exhibit typical symptoms of CRS, including high fever and elevated levels of certain cytokines implicated in CRS, such as IL-1 and/or IL-6. Control of CRS in these mice may be accomplished by blocking the receptor for the cytokine using, for example, antibodies, depletion of cell types expressing the cytokine, or administration of an antagonist of the cytokine. As above, it was determined that monocytes are the main source of the pro-CRS cytokine IL-6, and depletion of monocytes eliminated CRS and protected the mice from death from CRS.

Other CRS animal models are known in the art and may also be used as deemed appropriate.

Methods for Inducing and Testing Cytokine Release Syndrome for Control Purposes

In one model, IL-7 may be directly injected into a mouse or other animal model to induce or initiate CRS for control purposes, as described herein. In yet another example, recombinant or transgenic IL-7 may be expressed in a cell to result in increased IL-7 signaling.

In a still further example, a constitutively signaling cytokine receptor, such as an IL-7 receptor, may be engineered into an immune effector cell such that the immune effector cell itself triggers IL-7 signaling, but is unresponsive to extracellular IL-7, and initiation of IL-7 signaling of surrounding lymphocytes is avoided. Additionally, co-expressing a constitutively signaling IL-7 receptor with a CAR recognizing a specific disease or tumor antigen results in increased T-cell proliferation, survival, and antitumor activity. A constitutively expressing IL-7 receptor is able to transmit IL-7 signaling without the need for IL-7 ligand or the common gamma γ_(c) chain, a component of the native IL-7 receptor, along with IL-7Rα. This can be accomplished by engineering cysteine and/or proline into the transmembrane domain of the IL-7Rα chain, which results in homodimerization of IL-7Rα and subsequent phosphorylation of JAK1/JAK1, which then activates downstream signaling of IL-7.

An example of a method for making and testing a genome-edited CAR-T cell deficient at inducing CRS by insertion of selectable marker into gene edited locus is provided below.

Example 9—Insertion of CAR into T Cell Receptor Gene

A CAR or any protein of interest may be inserted into the gene for the T cell receptor. MacLeod et al. (“Integration of a CD19 CAR into the TCR Alpha Chain Locus Streamlines Production of Allogeneic Gene-Edited CAR T Cells,” Molec Therapy 25(4):P949-961, 2017) reports the generation of allogeneic CAR T cells by targeting the insertion of a CAR transgene directly into the native TCR locus using an engineered homing endonuclease and an AAV donor template. Anti-CD19 CAR T cells produced in this manner do not express the endogenous cell-surface TCR, exhibit potent effector functions in vitro, and mediate clearance of CD19+ tumors in an in vivo mouse model. The resulting gene-edited CAR T cells exhibit potent anti-tumor activity in vitro and in vivo in preclinical models, suggesting that these cells have potential for safe and efficacious use as adoptive cellular therapy in unrelated patients with CD19+ hematological malignancies.

Example 10—Anti-Cytokine/chemokineAntibodies to Reduce CRS

Introduction of immune effector cells to a patient or subject for treatment of cancer often results in CRS due to the production and secretion of cytokines and/or chemokines by the immune effector cells. One way to prevent CRS is to administer antibodies recognizing a specific CRS-inducing cytokine or chemokine to the patient or subject such that the amount of circulating cytokine/chemokine is reduced. For example, as reported by Sachdeva et al., (J Biol Chem 294(14):5430-5437, 2019), administration of anti-GMCSF antibodies reduced the GMCSF secretion thereby effectively reducing CRS. Therefore, administering antibodies recognizing a specific cytokine and/or chemokine can prevent or reduce the occurrence of CRS in a patient or subject.

Example 11—Insertion of CAR into GMCSF Gene

One exemplary way to prevent CRS is to insert a CAR into a gene for a cytokine or chemokine that is involved in initiation or prolonging of CRS. Disruption or ablation of a cytokine or chemokine gene in a CAR-T or other immune effector cell prevents the initiation of CRS by that particular cytokine or chemokine. One example of such a gene is GMCSF, although other genes involved in initiating or prolonging CRS may also be disrupted in this or a similar manner as described herein. Disruption of the GMCSF gene is described at least in Sachdeva et al. (J Biol Chem 294(14):5430-5437, 2019) and a description of making and testing a CAR-T cell inserted into the GM-CSF gene is provided below. Briefly, a TALEN or other gene-editing enzyme may be designed or engineered to target a cytokine or chemokine gene of choice in a CAR-T cell, and the expression of the gene monitored by methods known in the art. Significant reduction in the expression and secretion of the cytokine or chemokine gene by the CAR-T cell was reported, which implies that the occurrence of CRS would be reduced. Additionally, this approach was found to simultaneously maintain both the proliferation capability and the anti-tumor activity of the CAR-T cell, as assessed by transwell assays and serial killing assays.

In addition to the use of gene editing to delete a gene such as GM-CSF, antibodies to a cytokine or chemokine causing or contributing to CRS may also be used. For example, an antibody recognizing the GM-CSF protein may be administered to a patient or subject receiving CAR-T therapy. This practice is known in the art, particularly for reduction of CRS as a result of IL-6 signaling using the IL-6R antagonist tocilizumab, however other antibodies or antagonists recognizing cytokines or chemokines, or antagonists of their receptors, may be used as deemed appropriate by a clinician. Appropriate antibodies will bind to the circulating cytokine or chemokine, and antagonists will bind to the native receptors for the cytokine or chemokine, thus preventing downstream CRS-promoting activities in the subject. In some instances, both of these approaches may be employed in a subject, i.e., insertion of a CAR into the gene for a cytokine or chemokine to inactivate the gene, and also administering antibodies against the same cytokine or chemokine to the subject. This approach has been shown to be effective while conferring no negative effects on the activity of the CAR-T cells in vivo or in vitro (Sterner et al., “GM-CSF inhibition reduces cytokine release syndrome and neuroinflammation but enhances CAR-T cell function in xenografts,” Blood 133:697-709, 2019).

Example 12—Method of Making and Testing Genome-Edited CAR-T Cells Deficient at Inducing CRS by Insertion of Selectable Marker into Gene Edited Loci

Inject tumor in SCID-Beige mice (3e6 Raji containing Luciferase) if performing in vivo CRS experiment. This should be completed 3 weeks prior to infusion of CAR-T into mice.

The following steps may be taken to provide a genome-edited, CRS-resistant, CAR-T cell in which the CAR is expressed from the gene edited loci with a selectable marker disclosed herein. It is not possible to select and purify edited cells based on the deletion of genes that encode internal or secreted proteins, thus a selectable marker is required to enrich for this gene modification. This example describes the making of a CD19CARTΔGMCSFΔCD3ε cell, in which the deletion of GM-CSF mitigates risk of CRS and deletion of CD3ε prevents TCR signaling and graft vs host disease (GvHD). As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Step 1: T Cell Activation (Day 0)

Purify T cells from leukapheresis chamber using a Miltenyi human PanT isolation kit. Resuspend in media. Count cells. Determine number of human T cell activation CD3/CD28 beads required to obtain 3:1 bead:cell ratio. Wash beads 2× with T cell media. Dilute cells at 1.256 cells/mL in hXcyte media. Add human T cell activation CD3/CD28 beads. Aliquot 4 mL/well of 1.256 cell/mL solution into 6 well plate. Incubate cells at 37° C.

Step 2: CRISPR (Day 2)

The target gene is genetically deleted and the CAR inserted into the gene edited loci. The DNA double-stranded break can be repaired using homology directed repair using a donor template to repair the break and insert the desired sequence into the edited loci. Target deletion may be accomplished by electroporating with Cas9 mRNA and gRNA against the target(s). The donor template may be a DNA plasmid, or a double-stranded linear DNA, or a single stranded-stranded linear DNA containing homology to the DNA surrounding the double-stranded breaks electroplated with the Cas9/gRNA. In this example the homology arms align to either side of the double-stranded break induced by gRNA GM-CSF. Additionally, a viral vector such as AAV may be used as the source of the donor template. Other techniques, however, could be used to induce DNA double strand breaks. These include other genome editing techniques such as TALENs and mega-nucleases.

The sequences of the gRNAs for GM-CSF and CD3ε are as follows:

hGMCSF gRNA: (SEQ ID NO: 50) 5′_2′OMe(U(ps)A(ps)C(ps))UCAGGUUCAGGAGACGCGUUUUA GAGCUAGAAAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGA AAAAGUGGCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U_3′ CD3ϵ gRNA: (SEQ ID NO: 47) 5′_2′OMe(A(ps)G(ps)G(ps))GCAUGUCAAUAUUACUGGUUUUA GAGCUAGAAAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGA AAAAGUGGCACCGAGUCGGUGC2′OMe(U(ps)U(ps)U(ps)U 3′

Nucleofection Sample ID gRNA#1 gRNA#2 Cas9 Buffer P3 UCART19 20 μg 20 μg gCD3ε 15 μg Cas9 100 μl gGM-CSF mRNA

Nucleofection Using Nucleofector 4D:

Perform nucleofection protocol as described above (Example 6), using 20 μg of each gRNA (gGM-CSF and gCD3ε) to each tube of 15 μg cas9 mRNA.

Step 3: Transduction of T Cells with AAV Vector Containing HDR Repair Construct to Introduce CAR and a Selectable Marker into GM-CSF Loci

Sequences for components of vectors described herein are provided in the sequence listing, such as including, but not limited to, SEQ ID NOs: 3048-3064. For example, recombinant AAV6 donor vector (FIG. 3 , containing ITR-Right homology arm (SEQ ID NO:51), EF1a promotor (SEQ ID NO:52), CAR19 p2a trCD34 (SEQ ID NO:53), Left homology arm (SEQ ID NO:54), ITR (SEQ ID NO:55), is added to the cell culture 2-4 hrs after electroporation with a MOI between 1×10⁴ and 1×10⁶.

Step 4: Assessment of CRISPR Activity and Td Efficiency (Day 10)

Take 5×10⁵ cells from each sample and analyze by flow cytometry. Wash samples with RB. Add 3 μl of anti-CD34 PE antibody (This detects the insertion TrCD34 tag into GM-CSF loci). Add 5 μl of CD3 APC and 2 μl of anti-FAB BV421 (detects CAR transduction). Wash. Perform Flow cytometry. Cells should be CD3ε-negative, CD34-positive and FAB+. Harvest T cells (Day 11).

Purification of CAR-T cells. TCR-negative cells can be purified using TCRa/b negative selection to remove TCR positive cells. GM-CSF deleted cells can be enriched using a CD34-positive selection on the Miltenyi Automacs. This enriches the GM-SCF− cells and removes TCR+ cells.

Step 5: Assessment of CAR-T Activity In Vivo

Inject 3×10⁷ CAR-T per mouse I.P. Assess serum cytokine levels. (Day 12, Day 13, Day 14) Measure serum cytokine levels using Luminex multiplex cytokine profiling assay to check for elevations in CRS related cytokines. Perform a 4 hr chromium release assay against targets cells (Raji) to assess in vitro activity (Day 11).

Example 13—Confirmation of GFP Expression with EGFP Integration into CD3e Locus of Jurkats Under Control of CD3e Promotor

Direct insertion of GFP into the CD3e locus of a Jurkat cell line may be performed using the method details below.

Days prior: Digest plasmid with PST1 (FIG. 4 ). Two fragments (3.5 kb and 2.6 kb) are generated upon digestion. Purify using gel extraction kit and ethanol precipitate. Resuspend at 500 ng/μl. This generates donor template ‘DNA’ in table below

Make and titre AAV. The sequence of the AAV is shown in FIG. 5 and provided in SEQ ID NOs:______. This generates donor template ‘AAV’ in the table below.

Donor template ‘plasmid’ is shown in the table below.

Day 0:

Harvest jurkats and count. Spin cells down @100 g for 10 mins. Transfer cells to 1.5 m microcentrifuge tube and wash in PBS. Spin cells down @100×g for 10 mins. Resuspend in pre-warmed buffer SE. Add 100 μl to tube containing gRNA/Cas9. Transfer to nucleocuvette and zap using the Jurkat program on 4D. Transfer to pre-warmed media in 2 ml respective media in a 6-well plate. Return to incubator and expand for 4 days.

TABLE 14 Nucleofector Cell Cas9 Donor Name Solution Cell line number mRNA gRNA template 1 WT — Jurkat 4 × 10⁶ — 20 μg CD3e — 2 3Δ SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e — 3 P-1ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e Plasmid 1ug 4 P-2ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e Plasmid 2ug 5 P-2ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e Plasmid 3ug 6 D-1ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e DNA 1ug 7 D-2ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e DNA 2ug 8 D-4ug SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e DNA 3ug 9 AAV Td SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e AAV 1e4 10 AAV Td SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e AAV 1e5 11 AAV Td SE Jurkat 4 × 10⁶ 15 μg 20 μg CD3e AAV 1e6

Day 4: FACS cells for GFP and CD3 APC. Assess editing efficiency by loss of CD3 and integration of the AAV-GFP donor by GFP fluorescence.

Example 14—Method of Making and Testing a Genome-Edited CAR-T Cells by Insertion of CAR into CD3e Loci

The following steps may be taken to provide a genome-edited CAR-T cell in which the car is expressed from the gene edited loci (CAR-T) disclosed herein. This example describes the making of a CD7CART ΔCD7 ΔCD3ε cell. As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Step 1: T Cell Activation (Day 0)

Purify T cells from leukapheresis chamber using Miltenyi human PanT isolation kit. Resuspend in media. Count cells. Determine number of human T cell activation CD3/CD28 beads required to obtain 3:1 bead:cell ratio. Wash beads 2× with T cell media. Dilute cells at 1.256 cells/mL in hXcyte media. Add human T cell activation CD3/CD28 beads. Aliquot 4 mL/well of 1.256 cell/mL solution into 6 well plate. Incubate cells at 37° C.

Step 2: CRISPR (Day 2)

The target gene is genetically deleted and the CAR inserted into the gene edited loci. The DNA double-stranded break can be repaired using homology-directed repair using a donor template to repair the break and insert the desired sequence into the edited loci. Target deletion may be accomplished by electroporating with Cas9 mRNA and gRNA against the target(s). The donor template may be a DNA plasmid, or double-stranded linear DNA, or single-stranded linear DNA containing homology to the DNA surrounding the double-stranded breaks electroporated with the Cas9/gRNA. Additionally, a viral vector such as AAV may be used as the source of the donor template. Other techniques, however, could be used to induce DNA double-stranded breaks. These include other genome editing techniques, such as TALENs and mega-nucleases.

Nucleofection Sample ID gRNA#1 gRNA#2 Cas9 Buffer P3 UCART7 20 μg gCD7 20 μg gCD3ε 15 μg Cas9 100 μl mRNA

Nucleofection Using Nucleofector 4D:

Perform nucleofection protocol as described above (Example 6), using 20 μg of each gRNA (gCD7 and gCD38) to each tube of 15 μg Cas9.

Step 3: Transduction of T Cells with AAV Vector Containing HDR Repair Construct

Recombinant AAV6 (or other serotypes of AAV) donor vector is added to the cell culture 2-4 hrs after electroporation with an MOI between 1×10⁴ and 1×10⁶.

Step 4: Assessment of CRISPR Activity and Td Efficiency (Day 10)

Take 5×10⁵ cells from each sample and analyze by flow cytometry. Wash samples with RB. Add 3 μl of anti-CD34 PE antibody (This detects the CAR, as the construct contains human truncated CD34). Add 5 μl of CD3 APC and 2 μl of CD7 BV421. Wash. Perform Flow cytometry. Cells should be CD3ε-negative, CD7-negative and CD34-positive. Harvest T cells (Day 11).

Purification of CAR-T cells. CD34+ (CAR+) and TCR-negative cells can be purified in a single step using a positive selection of CD34+ cells on a Miltenyi Automacs. This enriches the CAR+ cells and removes and TCR+ cells (as CAR insertion disrupts TCR signaling).

Step 5: Assessment of CAR-T Activity In Vivo

Inject tumor in NSG mice (5×10⁵ MOLT3 or HH: containing Luciferase) if performing in vivo imaging experiment (Day 7).

Image tumor burden in mouse using bioluminescent imaging. Inject 2×10⁶ CD34+CAR-T per mouse I.V. via tail vein or perform a 4 hr chromium release assay against targets cell (MOLT3 or HH) (Day 11). Those of skill in the art will appreciate that some flexibility is possible in the specified time frames.

Example 15—Cytokine/Chemokine Gene Silencing Using shRNA

Similar to siRNAs, short hairpin RNA can be used to knock down or eliminate expression of a cytokine/chemokine/transcription factor gene in an immune effector cell.

Cherkassky et al. (“Human CAR T cells with cell-intrinsic PD-1 checkpoint blockade resist tumor-mediated inhibition,” J Clin Investig 2016; 126:3130-3144) reported use of shRNA to knock down expression of immune checkpoint PD-1 in CD28 mesothelin-specific CAR-T cells, which showed enhanced proliferative function upon antigen stimulation, augmented cytotoxicity, and enhanced cytokine secretion. In addition, a CD19-specific CAR with a PD-1 shRNA lentiviral cassette has been tested for use in CD19-positive B-cell lymphoma. A list of useful shRNAs and their sequences is provided in Tables 15 and 16.

Table 15. 5′ to 3′ (Forward) shRNA Sequences for Silencing of Cytokine/Chemokine GC Genes to Reduce the Incidence of CRS

TABLE 16 3′ to 5′ (Reverse) shRNA sequences for Silencing of Cytokine/Chemokine Genes to Reduce the Incidence of CRS Target SEQ Gene ID Lo- Symbol shRNA Reverse Oligo Sequence NO: cation Gene ID No. A2M AATTCAAAAAAGGCGTCCCTATACCAAATAACTCGAGTTATTTGGTATAGGGACGCCT 2036 chr12 ENST00000318602.11 A2M AATTCAAAAAAGACTGCATCAATCGTCATAACTCGAGTTATGACGATTGATGCAGTCT 2037 chr12 ENST00000318602.11 A2M AATTCAAAAACCTCCAGACATCCTTGAAATACTCGAGTATTTCAAGGATGTCTGGAGG 2038 chr12 ENST00000318602.11 ACKR1 AATTCAAAAAATCCTGTGGGCCTGGTTTATTCTCGAGAATAAACCAGGCCCACAGGAT 2039 chr1 ENST00000368122.2 ACKR1 AATTCAAAAATGGCAGAAGCCCTGGCAATTTCTCGAGAAATTGCCAGGGCTTCTGCCA 2040 chr1 ENST00000368122.2 ACKR1 AATTCAAAAAGGCGGATGGTTGAGATCTATCCTCGAGGATAGATCTCAACCATCCGCC 2041 chr1 ENST00000368122.2 ACKR2 AATTCAAAAAGAGCACTCTTTATACTATTAACTCGAGTTAATAGTATAAAGAGTGCTC 2042 chr3 ENST00000422265.5 ACKR2 AATTCAAAAAGTGGAACTGCCACGCAGATTTCTCGAGAAATCTGCGTGGCAGTTCCAC 2043 chr3 ENST00000422265.5 ACKR2 AATTCAAAAACATTGGGTCTTCGGGAGTTTCCTCGAGGAAACTCCCGAAGACCCAATG 2044 chr3 ENST00000422265.5 ACKR3 AATTCAAAAACACTATTGGTGTACCTTATAACTCGAGTTATAAGGTACACCAATAGTG 2045 chr2 ENST00000272928.3 ACKR3 AATTCAAAAAGGCATAGTGCTGACATATATTCTCGAGAATATATGTCAGCACTATGCC 2046 chr2 ENST00000272928.3 ACKR3 AATTCAAAAAGCCGTTCCCTTCTCCATTATCCTCGAGGATAATGGAGAAGGGAACGGC 2047 chr2 ENST00000272928.3 ACVR1 AATTCAAAAATGATAATTCCCTCGACAAATTCTCGAGAATTTGTCGAGGGAATTATCA 2048 chr2 ENST00000263640.7 ACVR1 AATTCAAAAAGCAGAACGTATTTAGCCATTACTCGAGTAATGGCTAAATACGTTCTGC 2049 chr2 ENST00000263640.7 ACVR1 AATTCAAAAACTGGTCTGTCTTTGGATAATACTCGAGTATTATCCAAAGACAGACCAG 2050 chr2 ENST00000263640.7 ACVR2B AATTCAAAAAATGTCACGAGGCCTCTCATACCTCGAGGTATGAGAGGCCTCGTGACAT 2051 chr3 ENST00000352511.4 ACVR2B AATTCAAAAACCCAGCTCATGAATGACTTTGCTCGAGCAAAGTCATTCATGAGCTGGG 2052 chr3 ENST00000352511.4 ACVR2B AATTCAAAAACTTTGGCTTGGCTGTTCGATTCTCGAGAATCGAACAGCCAAGCCAAAG 2053 chr3 ENST00000352511.4 ACVRL1 AATTCAAAAACCGGGAGACTGAGATCTATAACTCGAGTTATAGATCTCAGTCTCCCGG 2054 chr12 ENST00000388922.8 ACVRL1 AATTCAAAAACAGGAGCACCTGATTCCTTTCCTCGAGGAAAGGAATCAGGTGCTCCTG 2055 chr12 ENST00000388922.8 ACVRL1 AATTCAAAAACGTGGAGATCTTCGGTACACACTCGAGTGTGTACCGAAGATCTCCACG 2056 chr12 ENST00000388922.8 ADIPOQ AATTCAAAAAGTTGGAGGCCTTTAGATATTACTCGAGTAATATCTAAAGGCCTCCAAC 2057 chr3 ENST00000320741.6 ADIPOQ AATTCAAAAAATGCTCATATCAATCCTATAACTCGAGTTATAGGATTGATATGAGCAT 2058 chr3 ENST00000320741.6 ADIPOQ AATTCAAAAAACGGTTAGGAAGTTGATTATTCTCGAGAATAATCAACTTCCTAACCGT 2059 chr3 ENST00000320741.6 AGER AATTCAAAAACACACTGCAGTCGGAGCTAATCTCGAGATTAGCTCCGACTGCAGTGTG 2060 chr6 ENST00000375076.8 AGER AATTCAAAAAGAAGCCAGAAATTGTAGATTCCTCGAGGAATCTACAATTTCTGGCTTC 2061 chr6 ENST00000375076.8 AGER AATTCAAAAATGCTGATCCTCCCTGAGATAGCTCGAGCTATCTCAGGGAGGATCAGCA 2062 chr6 ENST00000375076.8 AGRN AATTCAAAAAGAGTTCTGTGTGGAAGATAAACTCGAGTTTATCTTCCACACAGAACTC 2063 chr1 ENST00000379370.6 AGRN AATTCAAAAAGCGCACGTATGACAGTGATTGCTCGAGCAATCACTGTCATACGTGCGC 2064 chr1 ENST00000379370.6 AGRN AATTCAAAAAACGACGGAGTCACCTACGAAACTCGAGTTTCGTAGGTGACTCCGTCGT 2065 chr1 ENST00000379370.6 AHR AATTCAAAAACGGCATAGAGACCGACTTAATCTCGAGATTAAGTCGGTCTCTATGCCG 2066 chr7 ENST00000242057.8 AHR AATTCAAAAAGCGGCATAGAGACCGACTTAACTCGAGTTAAGTCGGTCTCTATGCCGC 2067 chr7 ENST00000242057.8 AHR AATTCAAAAAATCCACAGTCAGCCATAATAACTCGAGTTATTATGGCTGACTGTGGAT 2068 chr7 ENST00000242057.8 AHR AATTCAAAAAACTGCTTAAAGTTGGTATTAACTCGAGTTAATACCAACTTTAAGCAGT 2069 chr7 ENST00000242057.8 AIMP1 AATTCAAAAACAGCCTGATCTTCACACTAATCTCGAGATTAGTGTGAAGATCAGGCTG 2070 chr4 ENST00000358008.7 AIMP1 AATTCAAAAAAGAAGTAGATGTCGGAGAAATCTCGAGATTTCTCCGACATCTACTTCT 2071 chr4 ENST00000358008.7 AIMP1 AATTCAAAAAGCCAGAGTAACCCTGACTAATCTCGAGATTAGTCAGGGTTACTCTGGC 2072 chr4 ENST00000358008.7 AREG AATTCAAAAACCTCTTTCCAGTGGATCATAACTCGAGTTATGATCCACTGGAAAGAGG 2073 chr4 ENST00000395748.7 AREG AATTCAAAAATACTCGGCTCAGGCCATTATGCTCGAGCATAATGGCCTGAGCCGAGTA 2074 chr4 ENST00000395748.7 AREG AATTCAAAAAATTCACGGAGAATGCAAATATCTCGAGATATTTGCATTCTCCGTGAAT 2075 chr4 ENST00000395748.7 BCL6 AATTCAAAAATGTGCCACAGCAATATCTATTCTCGAGAATAGATATTGCTGTGGCACA 2076 chr3 ENST00000406870.6 BCL6 AATTCAAAAAACTGCGTTAAAGGCTCGATTTCTCGAGAAATCGAGCCTTTAACGCAGT 2077 chr3 ENST00000406870.6 BCL6 AATTCAAAAACCGGCTCAATAACATCGTTAACTCGAGTTAACGATGTTATTGAGCCGG 2078 chr3 ENST00000406870.6 BCL6 AATTCAAAAAACAAGCCAGCCGGCTCAATAACTCGAGTTATTGAGCCGGCTGGCTTGT 2079 chr3 ENST00000406870.6 BMP1 AATTCAAAAAACTGACGAGGACAGCTATATTCTCGAGAATATAGCTGTCCTCGTCAGT 2080 chr8 ENST00000306385.9 BMP1 AATTCAAAAAGCTCGTAAGTCCTCCATCAAACTCGAGTTTGATGGAGGACTTACGAGC 2081 chr8 ENST00000306385.9 BMP1 AATTCAAAAAACAGCTGTGCCTACGACTATCCTCGAGGATAGTCGTAGGCACAGCTGT 2082 chr8 ENST00000306385.9 BMP10 AATTCAAAAAAGCAAGACGGTGTCGACTTTACTCGAGTAAAGTCGACACCGTCTTGCT 2083 chr2 ENST00000295379.1 BMP10 AATTCAAAAAGCGTCGTCACCTACAAGTTTACTCGAGTAAACTTGTAGGTGACGACGC 2084 chr2 ENST00000295379.1 BMP10 AATTCAAAAACATGGCTGAACTTAGGCTATACTCGAGTATAGCCTAAGTTCAGCCATG 2085 chr2 ENST00000295379.1 BMP15 AATTCAAAAATACTACGCGATGGTCTCAATTCTCGAGAATTGAGACCATCGCGTAGTA 2086 chrX ENST00000252677.3 BMP15 AATTCAAAAAGCCTTCTTGTTACTCTATTTCCTCGAGGAAATAGAGTAACAAGAAGGC 2087 chrX ENST00000252677.3 BMP15 AATTCAAAAAATGGAACACAGGGCCCAAATGCTCGAGCATTTGGGCCCTGTGTTCCAT 2088 chrX ENST00000252677.3 BMP2 AATTCAAAAAGATCATCTGAACTCCACTAATCTCGAGATTAGTGGAGTTCAGATGATC 2089 chr20 ENST00000378827.4 BMP2 AATTCAAAAACCGGAGATTCTTCTTTAATTTCTCGAGAAATTAAAGAAGAATCTCCGG 2090 chr20 ENST00000378827.4 BMP2 AATTCAAAAACAAGATGCTTTAGGAAACAATCTCGAGATTGTTTCCTAAAGCATCTTG 2091 chr20 ENST00000378827.4 BMP3 AATTCAAAAACTTACAGGGACACCGGAATTTCTCGAGAAATTCCGGTGTCCCTGTAAG 2092 chr4 ENST00000282701.2 BMP3 AATTCAAAAAGGCCAAATCTCATCGAGATATCTCGAGATATCTCGATGAGATTTGGCC 2093 chr4 ENST00000282701.2 BMP3 AATTCAAAAAGTGGATTGAACCTCGGAATTGCTCGAGCAATTCCGAGGTTCAATCCAC 2094 chr4 ENST00000282701.2 BMP4 AATTCAAAAACCCTGGTCAATTCTGTCAATTCTCGAGAATTGACAGAATTGACCAGGG 2095 chr14 ENST00000245451.8 BMP4 AATTCAAAAATCCTTGAGGATAGACAGATATCTCGAGATATCTGTCTATCCTCAAGGA 2096 chr14 ENST00000245451.8 BMP4 AATTCAAAAAAGGGCCAGCATGTCAGGATTACTCGAGTAATCCTGACATGCTGGCCCT 2097 chr14 ENST00000245451.8 BMP5 AATTCAAAAATGGACGCAGTATCAACGTAAACTCGAGTTTACGTTGATACTGCGTCCA 2098 chr6 ENST00000370830.3 BMP5 AATTCAAAAACCAGAAGGATACGCTGCATTTCTCGAGAAATGCAGCGTATCCTTCTGG 2099 chr6 ENST00000370830.3 BMP5 AATTCAAAAAATGCCACCAACCACGCTATAGCTCGAGCTATAGCGTGGTTGGTGGCAT 2100 chr6 ENST00000370830.3 BMP6 AATTCAAAAAATACAGGAATATGGTTGTAAGCTCGAGCTTACAACCATATTCCTGTAT 2101 chr6 ENST00000283147.6 BMP6 AATTCAAAAACGCCGACAACAGAGTCGTAATCTCGAGATTACGACTCTGTTGTCGGCG 2102 chr6 ENST00000283147.6 BMP6 AATTCAAAAACTGTCTATCAAAGGTAGATTTCTCGAGAAATCTACCTTTGATAGACAG 2103 chr6 ENST00000283147.6 BMP7 AATTCAAAAAACGTTCCGGATCAGCGTTTATCTCGAGATAAACGCTGATCCGGAACGT 2104 chr20 ENST00000395863.7 BMP7 AATTCAAAAAACTCGTTTCCAGAGGTAATTACTCGAGTAATTACCTCTGGAAACGAGT 2105 chr20 ENST00000395863.7 BMP7 AATTCAAAAAACCATCGAGAGTTCCGGTTTGCTCGAGCAAACCGGAACTCTCGATGGT 2106 chr20 ENST00000395863.7 BMP8A AATTCAAAAAAGGGTGCAGTTAGCATATTAGCTCGAGCTAATATGCTAACTGCACCCT 2107 chr1 ENST00000331593.5 BMP8A AATTCAAAAAAGCACAGAAGTCCTATCTTAGCTCGAGCTAAGATAGGACTTCTGTGCT 2108 chr1 ENST00000331593.5 BMP8A AATTCAAAAAAGGTACAACACTGGCCATTTCCTCGAGGAAATGGCCAGTGTTGTACCT 2109 chr1 ENST00000331593.5 BMP8B AATTCAAAAACCAAGGCTACTCGGCCTATTACTCGAGTAATAGGCCGAGTAGCCTTGG 2110 chr1 ENST00000372827.7 BMP8B AATTCAAAAAGACCCTCACAACCACGTACATCTCGAGATGTACGTGGTTGTGAGGGTC 2111 chr1 ENST00000372827.7 BMP8B AATTCAAAAACGTTAACATGGTGGAGCGAGACTCGAGTCTCGCTCCACCATGTTAACG 2112 chr1 ENST00000372827.7 BMPR2 AATTCAAAAAGAACGGCTATGTGCGTTTAAACTCGAGTTTAAACGCACATAGCCGTTC 2113 chr2 ENST00000374580.8 BMPR2 AATTCAAAAAGCCTATGGAGTGAAATTATTTCTCGAGAAATAATTTCACTCCATAGGC 2114 chr2 ENST00000374580.8 BMPR2 AATTCAAAAAATTACCACGAGGAGATCATTACTCGAGTAATGATCTCCTCGTGGTAAT 2115 chr2 ENST00000374580.8 C10orf99 AATTCAAAAACATCATGTGAGGCTCTGTAAACTCGAGTTTACAGAGCCTCACATGATG 2116 chr10 ENST00000372126.3 C10orf99 AATTCAAAAACCCAACTCAACAAACCTGAAACTCGAGTTTCAGGTTTGTTGAGTTGGG 2117 chr10 ENST00000372126.3 C10orf99 AATTCAAAAAGCCATCAACTTTCAGAGCTATCTCGAGATAGCTCTGAAAGTTGATGGC 2118 chr10 ENST00000372126.3 C1QTNF4 AATTCAAAAAACACCGAGTTCGTCAACATTGCTCGAGCAATGTTGACGAACTCGGTGT 2119 chr11 ENST00000302514.3 C1QTNF4 AATTCAAAAAGCGTAAGACGCTGTCGGTTAACTCGAGTTAACCGACAGCGTCTTACGC 2120 chr11 ENST00000302514.3 C1QTNF4 AATTCAAAAACGAGGTGCAGGCCATGATTTACTCGAGTAAATCATGGCCTGCACCTCG 2121 chr11 ENST00000302514.3 C5 AATTCAAAAAACGATGGAGCCTGCGTTAATACTCGAGTATTAACGCAGGCTCCATCGT 2122 chr9 ENST00000223642.2 C5 AATTCAAAAATCCCGACTTCTGGTCTATTACCTCGAGGTAATAGACCAGAAGTCGGGA 2123 chr9 ENST00000223642.2 C5 AATTCAAAAAGCCCGAGAGAACAGCTTATATCTCGAGATATAAGCTGTTCTCTCGGGC 2124 chr9 ENST00000223642.2 CCL1 AATTCAAAAAGCAATCCTGTGTTACAGAAATCTCGAGATTTCTGTAACACAGGATTGC 2125 chr17 ENST00000225842.3 CCL1 AATTCAAAAACTGCTCCAATGAGGGCTTAATCTCGAGATTAAGCCCTCATTGGAGCAG 2126 chr17 ENST00000225842.3 CCL1 AATTCAAAAACCTGAGGGCAATCCTGTGTTACTCGAGTAACACAGGATTGCCCTCAGG 2127 chr17 ENST00000225842.3 CCL11 AATTCAAAAACCAACTCCAAAGCCATAAATACTCGAGTATTTATGGCTTTGGAGTTGG 2128 chr17 ENST00000305869.3 CCL11 AATTCAAAAACATTCTGAGGTAACCTCATTACTCGAGTAATGAGGTTACCTCAGAATG 2129 chr17 ENST00000305869.3 CCL11 AATTCAAAAATCCTCCATGAATATCAGTTATCTCGAGATAACTGATATTCATGGAGGA 2130 chr17 ENST00000305869.3 CCL13 AATTCAAAAATGGAATACTTCTACCATAATTCTCGAGAATTATGGTAGAAGTATTCCA 2131 chr17 ENST00000225844.6 CCL13 AATTCAAAAATCAAGCTGGAGTACGTGAAATCTCGAGATTTCACGTACTCCAGCTTGA 2132 chr17 ENST00000225844.6 CCL13 AATTCAAAAAACTCAACGTCCCATCTACTTGCTCGAGCAAGTAGATGGGACGTTGAGT 2133 chr17 ENST00000225844.6 CCL14 AATTCAAAAACCTAGGGACCAAGACTGAATCCTCGAGGATTCAGTCTTGGTCCCTAGG 2134 chr17 ENST00000618404.4 CCL14 AATTCAAAAACAGCGGATTATGGATTACTATCTCGAGATAGTAATCCATAATCCGCTG 2135 chr17 ENST00000618404.4 CCL14 AATTCAAAAACAAGCCCGGAATTGTCTTCATCTCGAGATGAAGACAATTCCGGGCTTG 2136 chr17 ENST00000618404.4 CCL15 AATTCAAAAAGCTGAAGCCCTACTCAATATACTCGAGTATATTGAGTAGGGCTTCAGC 2137 chr17 ENST00000617897.1 CCL15 AATTCAAAAAACAGAGTTAATGATGTCAAAGCTCGAGCTTTGACATCATTAACTCTGT 2138 chr17 ENST00000617897.1 CCL15 AATTCAAAAAATCCCGTGTTCACTCATGAAACTCGAGTTTCATGAGTGAACACGGGAT 2139 chr17 ENST00000617897.1 CCL16 AATTCAAAAAAGGAGAAGTATTTCGAATATTCTCGAGAATATTCGAAATACTTCTCCT 2140 chr17 ENST00000611905.1 CCL16 AATTCAAAAAAGGAACTTGTCCACGGTTAAACTCGAGTTTAACCGTGGACAAGTTCCT 2141 chr17 ENST00000611905.1 CCL16 AATTCAAAAACTGCCTGAAGTATTATGAGAACTCGAGTTCTCATAATACTTCAGGCAG 2142 chr17 ENST00000611905.1 CCL17 AATTCAAAAAGAGAGTGAAGAATGCAGTTAACTCGAGTTAACTGCATTCTTCACTCTC 2143 chr16 ENST00000219244.8 CCL17 AATTCAAAAAGAGTACTTCAAGGGAGCCATTCTCGAGAATGGCTCCCTTGAAGTACTC 2144 chr16 ENST00000219244.8 CCL17 AATTCAAAAAGCAAAGCCTTGAGAGGTCTTGCTCGAGCAAGACCTCTCAAGGCTTTGC 2145 chr16 ENST00000219244.8 CCL18 AATTCAAAAATCTATTGTTGAGCTGCATTATCTCGAGATAATGCAGCTCAACAATAGA 2146 chr17 ENST00000616054.1 CCL18 AATTCAAAAACCTTCAACTCTTCGTACATTCCTCGAGGAATGTACGAAGAGTTGAAGG 2147 chr17 ENST00000616054.1 CCL18 AATTCAAAAAGTCTATACCTCCTGGCAGATTCTCGAGAATCTGCCAGGAGGTATAGAC 2148 chr17 ENST00000616054.1 CCL19 AATTCAAAAAGAGTCAAGCATTGTGAATTATCTCGAGATAATTCACAATGCTTGACTC 2149 chr9 ENST00000311925.6 CCL19 AATTCAAAAAGCCGCAGCAGTTAACCTATGACTCGAGTCATAGGTTAACTGCTGCGGC 2150 chr9 ENST00000311925.6 CCL19 AATTCAAAAACCAACTCTGAGTGGCACCAATCTCGAGATTGGTGCCACTCAGAGTTGG 2151 chr9 ENST00000311925.6 CCL2 AATTCAAAAACCCAGTCACCTGCTGTTATAACTCGAGTTATAACAGCAGGTGACTGGG 2152 chr17 ENST00000225831.4 CCL2 AATTCAAAAACCCAGTCACCTGCTGTTATAACTCGAGTTATAACAGCAGGTGACTGGG 2153 chr17 ENST00000225831.4 CCL2 AATTCAAAAAGCTCGCGAGCTATAGAAGAATCTCGAGATTCTTCTATAGCTCGCGAGC 2154 chr17 ENST00000225831.4 CCL20 AATTCAAAAAAGTTGTCTGTGTGCGCAAATCCTCGAGGATTTGCGCACACAGACAACT 2155 chr2 ENST00000358813.4 CCL20 AATTCAAAAAGACCGTATTCTTCATCCTAAACTCGAGTTTAGGATGAAGAATACGGTC 2156 chr2 ENST00000358813.4 CCL20 AATTCAAAAAAGGGTTTAGTGCTTATCTAATCTCGAGATTAGATAAGCACTAAACCCT 2157 chr2 ENST00000358813.4 CCL21 AATTCAAAAACACTCTTTCTCCTGCTTTAACCTCGAGGTTAAAGCAGGAGAAAGAGTG 2158 chr9 ENST00000259607.6 CCL21 AATTCAAAAAGAGCTATGTGCAGACCCAAAGCTCGAGCTTTGGGTCTGCACATAGCTC 2159 chr9 ENST00000259607.6 CCL21 AATTCAAAAACCATCCCAGCTATCCTGTTCTCTCGAGAGAACAGGATAGCTGGGATGG 2160 chr9 ENST00000259607.6 CCL22 AATTCAAAAACCCTACCTCCCTGCCATTATACTCGAGTATAATGGCAGGGAGGTAGGG 2161 chr16 ENST00000219235.4 CCL22 AATTCAAAAAGCGTGGTGAAACACTTCTACTCTCGAGAGTAGAAGTGTTTCACCACGC 2162 chr16 ENST00000219235.4 CCL22 AATTCAAAAAATGTTGCTGACACCCAGAAAGCTCGAGCTTTCTGGGTGTCAGCAACAT 2163 chr16 ENST00000219235.4 CCL23 AATTCAAAAACACTCCTGGAGAGTTACTTTGCTCGAGCAAAGTAACTCTCCAGGAGTG 2164 chr17 ENST00000615050.1 CCL23 AATTCAAAAACCTTTCTCATGCTGCAGGATTCTCGAGAATCCTGCAGCATGAGAAAGG 2165 chr17 ENST00000615050.1 CCL23 AATTCAAAAAGAAGCTGGACACACGGATCAACTCGAGTTGATCCGTGTGTCCAGCTTC 2166 chr17 ENST00000615050.1 CCL24 AATTCAAAAAAGTGATCTTCACCACCAAGAACTCGAGTTCTTGGTGGTGAAGATCACT 2167 chr7 ENST00000222902.6 CCL24 AATTCAAAAAGTTCTTTGTTTCCAAGAGAATCTCGAGATTCTCTTGGAAACAAAGAAC 2168 chr7 ENST00000222902.6 CCL24 AATTCAAAAACCTGCTGCATGTTCTTTGTTTCTCGAGAAACAAAGAACATGCAGCAGG 2169 chr7 ENST00000222902.6 CCL25 AATTCAAAAAGCCGGATCTTTCTCCGATAAACTCGAGTTTATCGGAGAAAGATCCGGC 2170 chr19 ENST00000390669.7 CCL25 AATTCAAAAAGCTCCTGGATGCTCGAAATAACTCGAGTTATTTCGAGCATCCAGGAGC 2171 chr19 ENST00000390669.7 CCL25 AATTCAAAAACCCTCCTGATATCAGCTAATTCTCGAGAATTAGCTGATATCAGGAGGG 2172 chr19 ENST00000390669.7 CCL26 AATTCAAAAACACACGTGGGAGTGACATATCCTCGAGGATATGTCACTCCCACGTGTG 2173 chr7 ENST00000005180.8 CCL26 AATTCAAAAATCCGAAACAATTGTGACTCAGCTCGAGCTGAGTCACAATTGTTTCGGA 2174 chr7 ENST00000005180.8 CCL26 AATTCAAAAAGCTGTGATATTCACTACCAAACTCGAGTTTGGTAGTGAATATCACAGC 2175 chr7 ENST00000005180.8 CCL27 AATTCAAAAATTCGTGCTTCACCTGGCTCAACTCGAGTTGAGCCAGGTGAAGCACGAA 2176 chr9 ENST00000259631.4 CCL27 AATTCAAAAACCGAAAGCCACTCTCAGACAACTCGAGTTGTCTGAGAGTGGCTTTCGG 2177 chr9 ENST00000259631.4 CCL27 AATTCAAAAACAAGCTACTGAGGAAGGTCATCTCGAGATGACCTTCCTCAGTAGCTTG 2178 chr9 ENST00000259631.4 CCL28 AATTCAAAAACGGAGGTTTCACATCATATTTCTCGAGAAATATGATGTGAAACCTCCG 2179 chr5 ENST00000361115.4 CCL28 AATTCAAAAACACGAAACATACGGCCATAAACTCGAGTTTATGGCCGTATGTTTCGTG 2180 chr5 ENST00000361115.4 CCL28 AATTCAAAAATTAGAGAGTCTACAGATAAATCTCGAGATTTATCTGTAGACTCTCTAA 2181 chr5 ENST00000361115.4 CCL3 AATTCAAAAACCGGCAGATTCCACAGAATTTCTCGAGAAATTCTGTGGAATCTGCCGG 2182 chr17 ENST00000613922.1 CCL3 AATTCAAAAATTCGATTTCACAGTGTGTTTGCTCGAGCAAACACACTGTGAAATCGAA 2183 chr17 ENST00000613922.1 CCL3 AATTCAAAAACAACCAGTTCTCTGCATCACTCTCGAGAGTGATGCAGAGAACTGGTTG 2184 chr17 ENST00000613922.1 CCL4 AATTCAAAAAATGTGCCGTGTTATTGTATTACTCGAGTAATACAATAACACGGCACAT 2185 chr17 ENST00000615863.1 CCL4 AATTCAAAAATCCTGTCCCTTCTCTTAATTTCTCGAGAAATTAAGAGAAGGGACAGGA 2186 chr17 ENST00000615863.1 CCL4 AATTCAAAAACTGTGCTGATCCCAGTGAATCCTCGAGGATTCACTGGGATCAGCACAG 2187 chr17 ENST00000615863.1 CCL5 AATTCAAAAATGAACCTGAACTTACACAAATCTCGAGATTTGTGTAAGTTCAGGTTCA 2188 chr17 ENST00000603197.5 CCL5 AATTCAAAAACCTGCTGCTTTGCCTACATTGCTCGAGCAATGTAGGCAAAGCAGCAGG 2189 chr17 ENST00000603197.5 CCL5 AATTCAAAAACTACCACACAGCAGCAGTTACCTCGAGGTAACTGCTGCTGTGTGGTAG 2190 chr17 ENST00000603197.5 CCL7 AATTCAAAAACATAAAGCCTTGGATGTATATCTCGAGATATACATCCAAGGCTTTATG 2191 chr17 ENST00000378569.2 CCL7 AATTCAAAAAGCTGCTACAGATTTATCAATACTCGAGTATTGATAAATCTGTAGCAGC 2192 chr17 ENST00000378569.2 CCL7 AATTCAAAAATCTAAGGAATATGAGCTTTATCTCGAGATAAAGCTCATATTCCTTAGA 2193 chr17 ENST00000378569.2 CCL8 AATTCAAAAAGCTGCTTTAACGTGATCAATACTCGAGTATTGATCACGTTAAAGCAGC 2194 chr17 ENST00000394620.1 CCL8 AATTCAAAAACAGGTGCAGTGTGACATTATTCTCGAGAATAATGTCACACTGCACCTG 2195 chr17 ENST00000394620.1 CCL8 AATTCAAAAATTGTACTGCTGTTGTTGAAATCTCGAGATTTCAACAACAGCAGTACAA 2196 chr17 ENST00000394620.1 CCR1 AATTCAAAAAATTCTGCTAAGACGACCAAATCTCGAGATTTGGTCGTCTTAGCAGAAT 2197 chr3 ENST00000296140.3 CCR1 AATTCAAAAAATCTGCTACACAGGGATTATACTCGAGTATAATCCCTGTGTAGCAGAT 2198 chr3 ENST00000296140.3 CCR1 AATTCAAAAACCTCTGTACTCCTTGGTATTTCTCGAGAAATACCAAGGAGTACAGAGG 2199 chr3 ENST00000296140.3 CCR2 AATTCAAAAAACGGTGCTCCCTGTCATAAATCTCGAGATTTATGACAGGGAGCACCGT 2200 chr3 ENST00000445132.2 CCR2 AATTCAAAAACTTCTGGACTCCCTATAATATCTCGAGATATTATAGGGAGTCCAGAAG 2201 chr3 ENST00000445132.2 CCR2 AATTCAAAAAGCTGTATCACATCGGTTATTTCTCGAGAAATAACCGATGTGATACAGC 2202 chr3 ENST00000445132.2 CCR3 AATTCAAAAAATACAGGAGGCTCCGAATTATCTCGAGATAATTCGGAGCCTCCTGTAT 2203 chr3 ENST00000357422.2 CCR3 AATTCAAAAACCCAGAGGATACAGTATATAGCTCGAGCTATATACTGTATCCTCTGGG 2204 chr3 ENST00000357422.2 CCR3 AATTCAAAAATAGCAGCTCTTCCTGAATTTACTCGAGTAAATTCAGGAAGAGCTGCTA 2205 chr3 ENST00000357422.2 CCR5 AATTCAAAAAACTCTTGACAGGGCTCTATTTCTCGAGAAATAGAGCCCTGTCAAGAGT 2206 chr3 ENST00000292303.4 CCR5 AATTCAAAAACGAGCGAGCAAGCTCAGTTTACTCGAGTAAACTGAGCTTGCTCGCTCG 2207 chr3 ENST00000292303.4 CCR5 AATTCAAAAATCCATACAGTCAGTATCAATTCTCGAGAATTGATACTGACTGTATGGA 2208 chr3 ENST00000292303.4 CCR6 AATTCAAAAAGGTCTATGACAGACGTCTATCCTCGAGGATAGACGTCTGTCATAGACC 2209 chr6 ENST00000341935.9 CCR6 AATTCAAAAACGACTCCAGTGAAGATTATTTCTCGAGAAATAATCTTCACTGGAGTCG 2210 chr6 ENST00000341935.9 CCR6 AATTCAAAAATCGACTCCAGTGAAGATTATTCTCGAGAATAATCTTCACTGGAGTCGA 2211 chr6 ENST00000341935.9 CCR7 AATTCAAAAAGATGAGGTCACGGACGATTACCTCGAGGTAATCGTCCGTGACCTCATC 2212 chr17 ENST00000246657.2 CCR7 AATTCAAAAAGCTGGTCGTGTTGACCTATATCTCGAGATATAGGTCAACACGACCAGC 2213 chr17 ENST00000246657.2 CCR7 AATTCAAAAACGTGTTGACCTATATCTATTTCTCGAGAAATAGATATAGGTCAACACG 2214 chr17 ENST00000246657.2 CD109 AATTCAAAAAGCCGATCCTTACATAGATATTCTCGAGAATATCTATGTAAGGATCGGC 2215 chr6 ENST00000287097.5 CD109 AATTCAAAAACCCGGAGGAAATGTGACTATTCTCGAGAATAGTCACATTTCCTCCGGG 2216 chr6 ENST00000287097.5 CD109 AATTCAAAAACCGCTTATCATTTGAGACCAACTCGAGTTGGTCTCAAATGATAAGCGG 2217 chr6 ENST00000287097.5 CD27 AATTCAAAAACTTACCTTATGTCAGTGAGATCTCGAGATCTCACTGACATAAGGTAAG 2218 chr12 ENST00000266557.3 CD27 AATTCAAAAAGCACTGTAACTCTGGTCTTCTCTCGAGAGAAGACCAGAGTTACAGTGC 2219 chr12 ENST00000266557.3 CD27 AATTCAAAAACCACCCACTTACCTTATGTCACTCGAGTGACATAAGGTAAGTGGGTGG 2220 chr12 ENST00000266557.3 CD27 AATTCAAAAAGCCAGATGTGTGAGCCAGGAACTCGAGTTCCTGGCTCACACATCTGGC 2221 chr12 ENST00000266557.3 CD28 AATTCAAAAACCTCCAGAATTTGTATGTTAACTCGAGTTAACATACAAATTCTGGAGG 2222 ch2 ENST00000458610.6 CD28 AATTCAAAAACAACCTTAGCTGCAAGTATTCCTCGAGGAATACTTGCAGCTAAGGTTG 2223 ch2 ENST00000458610.6 CD28 AATTCAAAAATGGAGTCCTGGCTTGCTATAGCTCGAGCTATAGCAAGCCAGGACTCCA 2224 ch2 ENST00000458610.6 CD28 AATTCAAAAACCTCCTCCTTACCTAGACAATCTCGAGATTGTCTAGGTAAGGAGGAGG 2225 ch2 ENST00000458610.6 CD36 AATTCAAAAAAGAACCTATTGATGGATTAAACTCGAGTTTAATCCATCAATAGGTTCT 2226 chr7 ENST00000309881.11 CD36 AATTCAAAAAGCCATAATCGACACATATAAACTCGAGTTTATATGTGTCGATTATGGC 2227 chr7 ENST00000309881.11 CD36 AATTCAAAAAACGGCTGCAGGTCAACCTATTCTCGAGAATAGGTTGACCTGCAGCCGT 2228 chr7 ENST00000309881.11 CD4 AATTCAAAAACCTGATCATCAAGAATCTTAACTCGAGTTAAGATTCTTGATGATCAGG 2229 chr12 ENST00000011653.8 CD4 AATTCAAAAAAGAGCGGATGTCTCAGATCAACTCGAGTTGATCTGAGACATCCGCTCT 2230 chr12 ENST00000011653.8 CD4 AATTCAAAAACCACTCGCCTTTACAGTTGAACTCGAGTTCAACTGTAAAGGCGAGTGG 2231 chr12 ENST00000011653.8 CD40LG AATTCAAAAAGGGAAACAGCTGACCGTTAAACTCGAGTTTAACGGTCAGCTGTTTCCC 2232 chrX ENST00000370629.6 CD40LG AATTCAAAAATTCGAGTCAAGCTCCATTTATCTCGAGATAAATGGAGCTTGACTCGAA 2233 chrX ENST00000370629.6 CD40LG AATTCAAAAATGACGCTGGGAGTCTTCATAACTCGAGTTATGAAGACTCCCAGCGTCA 2234 chrX ENST00000370629.6 CD70 AATTCAAAAACCATCGTGATGGCATCTACATCTCGAGATGTAGATGCCATCACGATGG 2235 chr19 ENST00000245903.3 CD70 AATTCAAAAACAGCTACGTATCCATCGTGATCTCGAGATCACGATGGATACGTAGCTG 2236 chr19 ENST00000245903.3 CD70 AATTCAAAAACCAACCTCACTGGGACACTTTCTCGAGAAAGTGTCCCAGTGAGGTTGG 2237 chr19 ENST00000245903.3 CD74 AATTCAAAAACAAGTCGGAACAGCAGATAACCTCGAGGTTATCTGCTGTTCCGACTTG 2238 chr5 ENST00000009530.11 CD74 AATTCAAAAAGAGAACCTGAGACACCTTAAGCTCGAGCTTAAGGTGTCTCAGGTTCTC 2239 chr5 ENST00000009530.11 CD74 AATTCAAAAACCACACAGCTACAGCTTTCTTCTCGAGAAGAAAGCTGTAGCTGTGTGG 2240 chr5 ENST00000009530.11 CD8A AATTCAAAAAGCTGGACTTCGCCTGTGATATCTCGAGATATCACAGGCGAAGTCCAGC 2241 ch2 ENST00000409511.6 CD8A AATTCAAAAAGTGTATTCATTCTCATGATTACTCGAGTAATCATGAGAATGAATACAC 2242 ch2 ENST00000409511.6 CD8A AATTCAAAAACCAGAGACAGCTTGATCAAAGCTCGAGCTTTGATCAAGCTGTCTCTGG 2243 ch2 ENST00000409511.6 CD8A AATTCAAAAACCTTCTCCTGTCACTGGTTATCTCGAGATAACCAGTGACAGGAGAAGG 2244 ch2 ENST00000409511.6 CER1 AATTCAAAAAGAGAAGATGCTGTCCAGATTTCTCGAGAAATCTGGACAGCATCTTCTC 2245 chr9 ENST00000380911.3 CER1 AATTCAAAAACCAGCCGATAGATGGAATGAACTCGAGTTCATTCCATCTATCGGCTGG 2246 chr9 ENST00000380911.3 CER1 AATTCAAAAACAAGAAATTCTGGCACCACTTCTCGAGAAGTGGTGCCAGAATTTCTTG 2247 chr9 ENST00000380911.3 CHRD AATTCAAAAAACGTCCTGCAAAGTGTCCTTTCTCGAGAAAGGACACTTTGCAGGACGT 2248 chr3 ENST00000204604.5 CHRD AATTCAAAAAACTGATCCAGAGCTGGAGAAACTCGAGTTTCTCCAGCTCTGGATCAGT 2249 chr3 ENST00000204604.5 CHRD AATTCAAAAACGGCTGCTGAAGGGATTCTATCTCGAGATAGAATCCCTTCAGCAGCCG 2250 chr3 ENST00000204604.5 CKLF AATTCAAAAACCTTTGCTTGTGTTTGCACTTCTCGAGAAGTGCAAACACAAGCAAAGG 2251 chr16 ENST00000264001.8 CKLF AATTCAAAAACCCTGAACCATATATTGTTATCTCGAGATAACAATATATGGTTCAGGG 2252 chr16 ENST00000264001.8 CKLF AATTCAAAAATGGATTTGAAGTCACCGTTATCTCGAGATAACGGTGACTTCAAATCCA 2253 chr16 ENST00000264001.8 CLCF1 AATTCAAAAAGAAACAAACATGGTGGCAATTCTCGAGAATTGCCACCATGTTTGTTTC 2254 chr11 ENST00000312438.7 CLCF1 AATTCAAAAACCACAGGATTTCCTGAAAGTTCTCGAGAACTTTCAGGAAATCCTGTGG 2255 chr11 ENST00000312438.7 CLCF1 AATTCAAAAACATGGTGGCAATTCTACACAACTCGAGTTGTGTAGAATTGCCACCATG 2256 chr11 ENST00000312438.7 CMTM1 AATTCAAAAACACCACTTGCTGACCTATTTACTCGAGTAAATAGGTCAGCAAGTGGTG 2257 chr16 ENST00000379500.6 CMTM1 AATTCAAAAAGACCTATTTACATTGGCCCTTCTCGAGAAGGGCCAATGTAAATAGGTC 2258 chr16 ENST00000379500.6 CMTM1 AATTCAAAAAGCTGTGTTCCTTTCAGTAGTTCTCGAGAACTACTGAAAGGAACACAGC 2259 chr16 ENST00000379500.6 CMTM2 AATTCAAAAAGTAAGGAGCCATCGGACAAACCTCGAGGTTTGTCCGATGGCTCCTTAC 2260 chr16 ENST00000268595.2 CMTM2 AATTCAAAAACTTACTTGCTGTGATCCTTATCTCGAGATAAGGATCACAGCAAGTAAG 2261 chr16 ENST00000268595.2 CMTM2 AATTCAAAAACATAAGGAGCCATCGGACAAACTCGAGTTTGTCCGATGGCTCCTTATG 2262 chr16 ENST00000268595.2 CMTM3 AATTCAAAAACATCGTGTTTGCAACTGATTTCTCGAGAAATCAGTTGCAAACACGATG 2263 chr16 ENST00000361909.8 CMTM3 AATTCAAAAAGCTTCTTAACAGATGGCATTTCTCGAGAAATGCCATCTGTTAAGAAGC 2264 chr16 ENST00000361909.8 CMTM3 AATTCAAAAAGCTTCTTAACAGATGGCATTTCTCGAGAAATGCCATCTGTTAAGAAGC 2265 chr16 ENST00000361909.8 CMTM4 AATTCAAAAACAACTGGAATCTGACAGATTTCTCGAGAAATCTGTCAGATTCCAGTTG 2266 chr16 ENST00000394106.6 CMTM4 AATTCAAAAAGACTGGCGTCTTGCTGATTATCTCGAGATAATCAGCAAGACGCCAGTC 2267 chr16 ENST00000394106.6 CMTM4 AATTCAAAAAGCAGAAATTGCTGCCGTGATACTCGAGTATCACGGCAGCAATTTCTGC 2268 chr16 ENST00000394106.6 CMTM5 AATTCAAAAACAAGATCTACCGGACTGAGATCTCGAGATCTCAGTCCGGTAGATCTTG 2269 chr14 ENST00000359320.7 CMTM5 AATTCAAAAACCTGACCCTCATCATCTTCATCTCGAGATGAAGATGATGAGGGTCAGG 2270 chr14 ENST00000359320.7 CMTM5 AATTCAAAAACTTCCTCTATGCCACCCAGTACTCGAGTACTGGGTGGCATAGAGGAAG 2271 chr14 ENST00000359320.7 CMTM6 AATTCAAAAAGCCCTCACTGAGCCACTTAATCTCGAGATTAAGTGGCTCAGTGAGGGC 2272 chr3 ENST00000205636.3 CMTM6 AATTCAAAAACCCAAGACAGTGAAAGTAATTCTCGAGAATTACTTTCACTGTCTTGGG 2273 chr3 ENST00000205636.3 CMTM6 AATTCAAAAACCCAAGACAGTGAAAGTAATTCTCGAGAATTACTTTCACTGTCTTGGG 2274 chr3 ENST00000205636.3 CMTM7 AATTCAAAAACTGCTGAAAGTGGCGCAAATGCTCGAGCATTTGCGCCACTTTCAGCAG 2275 chr3 ENST00000334983.9 CMTM7 AATTCAAAAACAAAGCCCTGTCCTAATTTATCTCGAGATAAATTAGGACAGGGCTTTG 2276 chr3 ENST00000334983.9 CMTM7 AATTCAAAAACCTGTCGATCTTTGGTTTCATCTCGAGATGAAACCAAAGATCGACAGG 2277 chr3 ENST00000334983.9 CMTM8 AATTCAAAAATGCTGGTATGGACGCTTATTGCTCGAGCAATAAGCGTCCATACCAGCA 2278 chr3 ENST00000307526.3 CMTM8 AATTCAAAAAGCAAAGTGTTGTAGCTTATAACTCGAGTTATAAGCTACAACACTTTGC 2279 chr3 ENST00000307526.3 CMTM8 AATTCAAAAAATATTCCCAGAGAATTGTATTCTCGAGAATACAATTCTCTGGGAATAT 2280 chr3 ENST00000307526.3 CNTF AATTCAAAAAGTAACCTCTACAGGCATTTAACTCGAGTTAAATGCCTGTAGAGGTTAC 2281 chr11 ENST00000361987.5 CNTF AATTCAAAAAGTTGAAGGACTACAGGTATTTCTCGAGAAATACCTGTAGTCCTTCAAC 2282 chr11 ENST00000361987.5 CNTF AATTCAAAAAGGTGACTTCCATCAAGCTATACTCGAGTATAGCTTGATGGAAGTCACC 2283 chr11 ENST00000361987.5 CNTFR AATTCAAAAACATTCTCTTCAGACACAATTTCTCGAGAAATTGTGTCTGAAGAGAATG 2284 chr9 ENST00000351266.8 CNTFR AATTCAAAAAGCATTCTCTTCAGACACAATTCTCGAGAATTGTGTCTGAAGAGAATGC 2285 chr9 ENST00000351266.8 CNTFR AATTCAAAAAGCCGGGAAGGAGTACATTATCCTCGAGGATAATGTACTCCTTCCCGGC 2286 chr9 ENST00000351266.8 COPS5 AATTCAAAAACTAAGGATCACCATTACTTTACTCGAGTAAAGTAATGGTGATCCTTAG 2287 chr8 ENST00000357849.8 COPS5 AATTCAAAAACCAGACTATTCCACTTAATAACTCGAGTTATTAAGTGGAATAGTCTGG 2288 chr8 ENST00000357849.8 COPS5 AATTCAAAAACAGTCTCTGAGAAGTACTTTACTCGAGTAAAGTACTTCTCAGAGACTG 2289 chr8 ENST00000357849.8 CRLF1 AATTCAAAAACGATGTACTCACGCTGGATATCTCGAGATATCCAGCGTGAGTACATCG 2290 chr19 ENST00000392386.7 CRLF1 AATTCAAAAACGATGTACTCACGCTGGATATCTCGAGATATCCAGCGTGAGTACATCG 2291 chr19 ENST00000392386.7 CRLF1 AATTCAAAAACCCAGAGAAACCCGTCAACATCTCGAGATGTTGACGGGTTTCTCTGGG 2292 chr19 ENST00000392386.7 CSF1 AATTCAAAAATCTCCTGGTACAAGACATAATCTCGAGATTATGTCTTGTACCAGGAGA 2293 chr1 ENST00000329608.10 CSF1 AATTCAAAAAGTCGGCCTGATTTCCCGTAAACTCGAGTTTACGGGAAATCAGGCCGAC 2294 chr1 ENST00000329608.10 CSF1 AATTCAAAAATTGACAAGGACTGGAATATTTCTCGAGAAATATTCCAGTCCTTGTCAA 2295 chr1 ENST00000329608.10 CSF1R AATTCAAAAAGTGAACAGCAAGTTCTATAAACTCGAGTTTATAGAACTTGCTGTTCAC 2296 chr5 ENST00000286301.7 CSF1R AATTCAAAAAACAGGAGAGAGCGGGACTATACTCGAGTATAGTCCCGCTCTCTCCTGT 2297 chr5 ENST00000286301.7 CSF1R AATTCAAAAAGCTGCTATTGTACAAGTATAACTCGAGTTATACTTGTACAATAGCAGC 2298 chr5 ENST00000286301.7 CSF2 AATTCAAAAAGGAGCTGCTCTCTCATGAAACCTCGAGGTTTCATGAGAGAGCAGCTCC 2299 chr5 ENST00000296871.3 CSF2 AATTCAAAAACCCAGATTATCACCTTTGAAACTCGAGTTTCAAAGGTGATAATCTGGG 2300 chr5 ENST00000296871.3 CSF2 AATTCAAAAAGAAGTCATCTCAGAAATGTTTCTCGAGAAACATTTCTGAGATGACTTC 2301 chr5 ENST00000296871.3 CSF3 AATTCAAAAAGTCTATTTAAGCCTCATATTTCTCGAGAAATATGAGGCTTAAATAGAC 2302 chr17 ENST00000225474.6 CSF3 AATTCAAAAAGATAGGTAAATACCAAGTATTCTCGAGAATACTTGGTATTTACCTATC 2303 chr17 ENST00000225474.6 CSF3 AATTCAAAAAGCTTAGAGCAAGTGAGGAAGACTCGAGTCTTCCTCACTTGCTCTAAGC 2304 chr17 ENST00000225474.6 CSF3R AATTCAAAAACAGCCAGGCCTGCACATAAATCTCGAGATTTATGTGCAGGCCTGGCTG 2305 chr1 ENST00000361632.8 CSF3R AATTCAAAAACTATGCCTACTCTCAAGAAATCTCGAGATTTCTTGAGAGTAGGCATAG 2306 chr1 ENST00000361632.8 CSF3R AATTCAAAAACCAGCTTCACTCTGAAGAGTTCTCGAGAACTCTTCAGAGTGAAGCTGG 2307 chr1 ENST00000361632.8 CTF1 AATTCAAAAAGAGCAGCTGCTCCAGGAATATCTCGAGATATTCCTGGAGCAGCTGCTC 2308 chr16 ENST00000279804.2 CTF1 AATTCAAAAAGTCTCTCCTTCCGCTTCTTTGCTCGAGCAAAGAAGCGGAAGGAGAGAC 2309 chr16 ENST00000279804.2 CTF1 AATTCAAAAATGTCTGTCTGTCTGCTCTTAGCTCGAGCTAAGAGCAGACAGACAGACA 2310 chr16 ENST00000279804.2 CX3CL1 AATTCAAAAACCCGGAGCTGTGGTAGTAATTCTCGAGAATTACTACCACAGCTCCGGG 2311 chr16 ENST00000006053.6 CX3CL1 AATTCAAAAAGCTGCTGCCCTAACTCGAAATCTCGAGATTTCGAGTTAGGGCAGCAGC 2312 chr16 ENST00000006053.6 CX3CL1 AATTCAAAAACGGTGTGACGAAATGCAACATCTCGAGATGTTGCATTTCGTCACACCG 2313 chr16 ENST00000006053.6 CX3CR1 AATTCAAAAATGGCCTGTGTCTAGTTGTTTGCTCGAGCAAACAACTAGACACAGGCCA 2314 chr3 ENST00000399220.2 CX3CR1 AATTCAAAAATGGGATCCCTCATCCTCATACCTCGAGGTATGAGGATGAGGGATCCCA 2315 chr3 ENST00000399220.2 CX3CR1 AATTCAAAAAGCTTTGCTCATCCACTATCAACTCGAGTTGATAGTGGATGAGCAAAGC 2316 chr3 ENST00000399220.2 CXCL1 AATTCAAAAAACCTGCACACTGTCCTATTATCTCGAGATAATAGGACAGTGTGCAGGT 2317 chr4 ENST00000395761.3 CXCL1 AATTCAAAAAAGATGCTGAACAGTGACAAATCTCGAGATTTGTCACTGTTCAGCATCT 2318 chr4 ENST00000395761.3 CXCL1 AATTCAAAAAGTTCTCCAGTCATTATGTTAACTCGAGTTAACATAATGACTGGAGAAC 2319 chr4 ENST00000395761.3 CXCL10 AATTCAAAAAGTATATGTCAAGCCATAATTGCTCGAGCAATTATGGCTTGACATATAC 2320 chr4 ENST00000306602.2 CXCL10 AATTCAAAAAACTCTACCCTGGCACTATAATCTCGAGATTATAGTGCCAGGGTAGAGT 2321 chr4 ENST00000306602.2 CXCL10 AATTCAAAAACCTGTTAATCCAAGGTCTTTACTCGAGTAAAGACCTTGGATTAACAGG 2322 chr4 ENST00000306602.2 CXCL11 AATTCAAAAAGCTGGTTACCATCGGAGTTTACTCGAGTAAACTCCGATGGTAACCAGC 2323 chr4 ENST00000306621.7 CXCL11 AATTCAAAAAGCAGTGAAAGTGGCAGATATTCTCGAGAATATCTGCCACTTTCACTGC 2324 chr4 ENST00000306621.7 CXCL11 AATTCAAAAAGAAGCAAGCAAGGCTTATAATCTCGAGATTATAAGCCTTGCTTGCTTC 2325 chr4 ENST00000306621.7 CXCL12 AATTCAAAAAGCTTAGACTAAGGCCATTATTCTCGAGAATAATGGCCTTAGTCTAAGC 2326 chr10 ENST00000343575.10 CXCL12 AATTCAAAAACTCTCACTATACCAGTATAATCTCGAGATTATACTGGTATAGTGAGAG 2327 chr10 ENST00000343575.10 CXCL12 AATTCAAAAACAAACTGTGCCCTTCAGATTGCTCGAGCAATCTGAAGGGCACAGTTTG 2328 chr10 ENST00000343575.10 CXCL13 AATTCAAAAAGATTCCCTGATGCTGATATTTCTCGAGAAATATCAGCATCAGGGAATC 2329 chr4 ENST00000286758.4 CXCL13 AATTCAAAAAAGGAATCCATGTAGTAGATATCTCGAGATATCTACTACATGGATTCCT 2330 chr4 ENST00000286758.4 CXCL13 AATTCAAAAAAGGTGTTCTGGAGGTCTATTACTCGAGTAATAGACCTCCAGAACACCT 2331 chr4 ENST00000286758.4 CXCL14 AATTCAAAAAATTTGTCCATACGTCACTATACTCGAGTATAGTGACGTATGGACAAAT 2332 chr5 ENST00000337225.5 CXCL14 AATTCAAAAACAAAGGACTTTGCAGATTAAACTCGAGTTTAATCTGCAAAGTCCTTTG 2333 chr5 ENST00000337225.5 CXCL14 AATTCAAAAAGCGCAGGGTCTACGAAGAATACTCGAGTATTCTTCGTAGACCCTGCGC 2334 chr5 ENST00000337225.5 CXCL16 AATTCAAAAAACATCCAGCCTACACGTATTTCTCGAGAAATACGTGTAGGCTGGATGT 2335 chr17 ENST00000293778.10 CXCL16 AATTCAAAAATCTGAAGGTGCGAGGATTATACTCGAGTATAATCCTCGCACCTTCAGA 2336 chr17 ENST00000293778.10 CXCL16 AATTCAAAAATCCAGATCTGCCGGTTCATTACTCGAGTAATGAACCGGCAGATCTGGA 2337 chr17 ENST00000293778.10 CXCL17 AATTCAAAAAGCGCCCACTCTTCCAATTAAACTCGAGTTTAATTGGAAGAGTGGGCGC 2338 chr19 ENST00000601181.5 CXCL17 AATTCAAAAATCCAGAGCCTGCCAGCAATTTCTCGAGAAATTGCTGGCAGGCTCTGGA 2339 chr19 ENST00000601181.5 CXCL17 AATTCAAAAAAGAATGTGAGTGCAAAGATTGCTCGAGCAATCTTTGCACTCACATTCT 2340 chr19 ENST00000601181.5 CXCL2 AATTCAAAAACTTGCACACTCTCCCATTATACTCGAGTATAATGGGAGAGTGTGCAAG 2341 chr4 ENST00000508487.2 CXCL2 AATTCAAAAAGCAGATATTCTCTAGTCATTTCTCGAGAAATGACTAGAGAATATCTGC 2342 chr4 ENST00000508487.2 CXCL2 AATTCAAAAAATTTCTTCGTGATGACATATCCTCGAGGATATGTCATCACGAAGAAAT 2343 chr4 ENST00000508487.2 CXCL3 AATTCAAAAATTACGAGGGTTCTACTTATTTCTCGAGAAATAAGTAGAACCCTCGTAA 2344 chr4 ENST00000296026.4 CXCL3 AATTCAAAAAATTTAGTGGGAGACCATAATGCTCGAGCATTATGGTCTCCCACTAAAT 2345 chr4 ENST00000296026.4 CXCL3 AATTCAAAAAACTGACAGGAGAGAAGTAAGACTCGAGTCTTACTTCTCTCCTGTCAGT 2346 chr4 ENST00000296026.4 CXCL5 AATTCAAAAATGAATTGTAGGTGACTATTATCTCGAGATAATAGTCACCTACAATTCA 2347 chr4 ENST00000296027.4 CXCL5 AATTCAAAAACAGACCACGCAAGGAGTTCATCTCGAGATGAACTCCTTGCGTGGTCTG 2348 chr4 ENST00000296027.4 CXCL5 AATTCAAAAACGGGAAGGAAATTTGTCTTGACTCGAGTCAAGACAAATTTCCTTCCCG 2349 chr4 ENST00000296027.4 CXCL6 AATTCAAAAATTTACCCTAGGATGCTATTTACTCGAGTAAATAGCATCCTAGGGTAAA 2350 chr4 ENST00000226317.9 CXCL6 AATTCAAAAAGTTGCACTTGTTTACGCGTTACTCGAGTAACGCGTAAACAAGTGCAAC 2351 chr4 ENST00000226317.9 CXCL6 AATTCAAAAAGCTGTGGATTTCGTATGGAAACTCGAGTTTCCATACGAAATCCACAGC 2352 chr4 ENST00000226317.9 CXCL8 AATTCAAAAATGCGCCAACACAGAAATTATTCTCGAGAATAATTTCTGTGTTGGCGCA 2353 chr4 ENST00000307407.7 CXCL8 AATTCAAAAACAAGAGAATATCCGAACTTTACTCGAGTAAAGTTCGGATATTCTCTTG 2354 chr4 ENST00000307407.7 CXCL8 AATTCAAAAATGCACGGGAGAATATACAAATCTCGAGATTTGTATATTCTCCCGTGCA 2355 chr4 ENST00000307407.7 CXCL9 AATTCAAAAACCAAAGGAGGATGGCATATAACTCGAGTTATATGCCATCCTCCTTTGG 2356 chr4 ENST00000264888.5 CXCL9 AATTCAAAAACCAAACGTTAAGAATTGTTAACTCGAGTTAACAATTCTTAACGTTTGG 2357 chr4 ENST00000264888.5 CXCL9 AATTCAAAAAGATGTGAAGGAACTGATTAAACTCGAGTTTAATCAGTTCCTTCACATC 2358 chr4 ENST00000264888.5 CXCR1 AATTCAAAAACTTGGCACGTCATCGTGTTACCTCGAGGTAACACGATGACGTGCCAAG 2359 chr2 ENST00000295683.2 CXCR1 AATTCAAAAAACCCACTAACTGGCTAATTAGCTCGAGCTAATTAGCCAGTTAGTGGGT 2360 chr2 ENST00000295683.2 CXCR1 AATTCAAAAAGAGACACTCAACAAGTATGTTCTCGAGAACATACTTGTTGAGTGTCTC 2361 chr2 ENST00000295683.2 CXCR2 AATTCAAAAAGAAGCGCTACTTGGTCAAATTCTCGAGAATTTGACCAAGTAGCGCTTC 2362 chr2 ENST00000318507.6 CXCR2 AATTCAAAAAGCCACTAAATTGACACTTAAACTCGAGTTTAAGTGTCAATTTAGTGGC 2363 chr2 ENST00000318507.6 CXCR2 AATTCAAAAACCCTGGAAATCAACAAGTATTCTCGAGAATACTTGTTGATTTCCAGGG 2364 chr2 ENST00000318507.6 CXCR3 AATTCAAAAACCTTCTCATTTGGAAACTAAACTCGAGTTTAGTTTCCAAATGAGAAGG 2365 chrX ENST00000373693.3 CXCR3 AATTCAAAAACGCTACCTGAACATAGTTCATCTCGAGATGAACTATGTTCAGGTAGCG 2366 chrX ENST00000373693.3 CXCR3 AATTCAAAAAGAGTACAAGGCATGGCGTAGACTCGAGTCTACGCCATGCCTTGTACTC 2367 chrX ENST00000373693.3 CXCR4 AATTCAAAAACTATTCCCGACTTCATCTTTGCTCGAGCAAAGATGAAGTCGGGAATAG 2368 chr2 ENST00000409817.1 CXCR4 AATTCAAAAAGCGTGTAGTGAATCACGTAAACTCGAGTTTACGTGATTCACTACACGC 2369 chr2 ENST00000409817.1 CXCR4 AATTCAAAAACCTGTTCTTAAGACGTGATTTCTCGAGAAATCACGTCTTAAGAACAGG 2370 chr2 ENST00000409817.1 CXCR6 AATTCAAAAAGCTTGCTCATCTGGGTGATATCTCGAGATATCACCCAGATGAGCAAGC 2371 chr3 ENST00000304552.4 CXCR6 AATTCAAAAATACTGGGCATCTACACTATTACTCGAGTAATAGTGTAGATGCCCAGTA 2372 chr3 ENST00000304552.4 CXCR6 AATTCAAAAATTATCTATGGCAATGTCTTTACTCGAGTAAAGACATTGCCATAGATAA 2373 chr3 ENST00000304552.4 EBI3 AATTCAAAAATGAACTGTCACTGTGAGATATCTCGAGATATCTCACAGTGACAGTTCA 2374 chr19 ENST00000221847.5 EBI3 AATTCAAAAAATGTACTACTCTCTCCTTTACCTCGAGGTAAAGGAGAGAGTAGTACAT 2375 chr19 ENST00000221847.5 EBI3 AATTCAAAAAGCCTTTCATAACAGAGCACATCTCGAGATGTGCTCTGTTATGAAAGGC 2376 chr19 ENST00000221847.5 EDN1 AATTCAAAAACCATGAGAAACAGCGTCAAATCTCGAGATTTGACGCTGTTTCTCATGG 2377 chr6 ENST00000379375.5 EDN1 AATTCAAAAAGCTCGTCCCTGATGGATAAAGCTCGAGCTTTATCCATCAGGGACGAGC 2378 chr6 ENST00000379375.5 EDN1 AATTCAAAAAAGACAAGAAGTGCTGGAATTTCTCGAGAAATTCCAGCACTTCTTGTCT 2379 chr6 ENST00000379375.5 ELANE AATTCAAAAAGCACTGCGTGGCGAATGTAAACTCGAGTTTACATTCGCCACGCAGTGC 2380 chr19 ENST00000263621.1 ELANE AATTCAAAAATGCTCAACGACATCGTGATTCCTCGAGGAATCACGATGTCGTTGAGCA 2381 chr19 ENST00000263621.1 ELANE AATTCAAAAACAACGGGCTAATCCACGGAATCTCGAGATTCCGTGGATTAGCCCGTTG 2382 chr19 ENST00000263621.1 ENG AATTCAAAAAGCAGGTGTCAGCAAGTATGATCTCGAGATCATACTTGCTGACACCTGC 2383 chr9 ENST00000344849.4 ENG AATTCAAAAAGCAGGTGTCAGCAAGTATGATCTCGAGATCATACTTGCTGACACCTGC 2384 chr9 ENST00000344849.4 ENG AATTCAAAAAGTCTTGCAGAAACAGTCCATTCTCGAGAATGGACTGTTTCTGCAAGAC 2385 chr9 ENST00000344849.4 EPO AATTCAAAAACCCAGACACCAAAGTTAATTTCTCGAGAAATTAACTTTGGTGTCTGGG 2386 chr7 ENST00000252723.2 EPO AATTCAAAAATGCAGCTGCATGTGGATAAAGCTCGAGCTTTATCCACATGCAGCTGCA 2387 chr7 ENST00000252723.2 EPO AATTCAAAAAAGAGCAACTCTGAGATCTAAGCTCGAGCTTAGATCTCAGAGTTGCTCT 2388 chr7 ENST00000252723.2 FAM3B AATTCAAAAATTGGAACTCCCTTCCGAAATTCTCGAGAATTTCGGAAGGGAGTTCCAA 2389 chr21 ENST00000357985.6 FAM3B AATTCAAAAATAAATCCAACAGCCCATATTTCTCGAGAAATATGGGCTGTTGGATTTA 2390 chr21 ENST00000357985.6 FAM3B AATTCAAAAATCAGGTCTAGCTGGGTATTTACTCGAGTAAATACCCAGCTAGACCTGA 2391 chr21 ENST00000357985.6 FAM3C AATTCAAAAACTTGGTGTGTGCATGAGTATTCTCGAGAATACTCATGCACACACCAAG 2392 chr7 ENST00000359943.7 FAM3C AATTCAAAAAGAGGAGATGTGGCACCATTTACTCGAGTAAATGGTGCCACATCTCCTC 2393 chr7 ENST00000359943.7 FAM3C AATTCAAAAAGCCATACAAGATGGAACAATACTCGAGTATTGTTCCATCTTGTATGGC 2394 chr7 ENST00000359943.7 FAM3D AATTCAAAAACACCTAGTGAAATTCCTTAAACTCGAGTTTAAGGAATTTCACTAGGTG 2395 chr3 ENST00000358781.6 FAM3D AATTCAAAAACATGTACTCTGGAGATGTTATCTCGAGATAACATCTCCAGAGTACATG 2396 chr3 ENST00000358781.6 FAM3D AATTCAAAAACAATGTGGGCAGAGGCCTAAACTCGAGTTTAGGCCTCTGCCCACATTG 2397 chr3 ENST00000358781.6 FAS AATTCAAAAAGCGTATGACACATTGATTAAACTCGAGTTTAATCAATGTGTCATACGC 2398 chr10 ENST00000355740.6 FAS AATTCAAAAACCTGAAACAGTGGCAATAAATCTCGAGATTTATTGCCACTGTTTCAGG 2399 chr10 ENST00000355740.6 FAS AATTCAAAAACTATCATCCTCAAGGACATTACTCGAGTAATGTCCTTGAGGATGATAG 2400 chr10 ENST00000355740.6 FASLG AATTCAAAAAGACTAGAGGCTTGCATAATAACTCGAGTTATTATGCAAGCCTCTAGTC 2401 chr1 ENST00000367721.2 FASLG AATTCAAAAAACTGGGCTGTACTTTGTATATCTCGAGATATACAAAGTACAGCCCAGT 2402 chr1 ENST00000367721.2 FASLG AATTCAAAAATGAGCTCTCTCTGGTCAATTTCTCGAGAAATTGACCAGAGAGAGCTCA 2403 chr1 ENST00000367721.2 FGF2 AATTCAAAAAGAAACGAACTGGGCAGTATAACTCGAGTTATACTGCCCAGTTCGTTTC 2404 chr4 ENST00000608478.1 FGF2 AATTCAAAAATATAGCTCAGTTTGGATAATTCTCGAGAATTATCCAAACTGAGCTATA 2405 chr4 ENST00000608478.1 FGF2 AATTCAAAAATGAACGATTGGAATCTAATAACTCGAGTTATTAGATTCCAATCGTTCA 2406 chr4 ENST00000608478.1 FLT3LG AATTCAAAAACTGTCTGACTACCTGCTTCAACTCGAGTTGAAGCAGGTAGTCAGACAG 2407 chr19 ENST00000594009.5 FLT3LG AATTCAAAAATCCTCCGACTTCGCTGTCAAACTCGAGTTTGACAGCGAAGTCGGAGGA 2408 chr19 ENST00000594009.5 FLT3LG AATTCAAAAAGCTTCGTCCAGACCAACATCTCTCGAGAGATGTTGGTCTGGACGAAGC 2409 chr19 ENST00000594009.5 FOXP3 AATTCAAAAAAGCTGGAGTTCCGCAAGAAACCTCGAGGTTTCTTGCGGAACTCCAGCT 2410 chrX ENST00000376207.8 FOXP3 AATTCAAAAATCCTACCCACTGCTGGCAAATCTCGAGATTTGCCAGCAGTGGGTAGGA 2411 chrX ENST00000376207.8 FOXP3 AATTCAAAAATGTCCCTCACTCAACACAAACCTCGAGGTTTGTGTTGAGTGAGGGACA 2412 chrX ENST00000376207.8 FOXP3 AATTCAAAAACACACGCATGTTTGCCTTCTTCTCGAGAAGAAGGCAAACATGCGTGTG 2413 chrX ENST00000376207.8 FZD4 AATTCAAAAACGTGTGTGATTGCCTGTTATTCTCGAGAATAACAGGCAATCACACACG 2414 chr11 ENST00000531380.1 FZD4 AATTCAAAAATCTCAGTATGTGCTATAATATCTCGAGATATTATAGCACATACTGAGA 2415 chr11 ENST00000531380.1 FZD4 AATTCAAAAATTCTCAGTATGTGCTATAATACTCGAGTATTATAGCACATACTGAGAA 2416 chr11 ENST00000531380.1 GATA3 AATTCAAAAAAGCCTAAACGCGATGGATATACTCGAGTATATCCATCGCGTTTAGGCT 2417 chr10 ENST00000346208.4 GATA3 AATTCAAAAACCCAAGAACAGCTCGTTTAACCTCGAGGTTAAACGAGCTGTTCTTGGG 2418 chr10 ENST00000346208.4 GATA3 AATTCAAAAAGCCAAGAAGTTTAAGGAATATCTCGAGATATTCCTTAAACTTCTTGGC 2419 chr10 ENST00000346208.4 GATA3 AATTCAAAAACCCTGTAATTGTTGTTTGTATCTCGAGATACAAACAACAATTACAGGG 2420 chr10 ENST00000346208.4 GBP1 AATTCAAAAACCAGATGAGTACCTGACATACCTCGAGGTATGTCAGGTACTCATCTGG 2421 chr1 ENST00000370473.4 GBP1 AATTCAAAAACGACGAAAGGCATGTACCATACTCGAGTATGGTACATGCCTTTCGTCG 2422 chr1 ENST00000370473.4 GBP1 AATTCAAAAACGACGAAAGGCATGTACCATACTCGAGTATGGTACATGCCTTTCGTCG 2423 chr1 ENST00000370473.4 GDF1 AATTCAAAAAGTTCACCAAGCTCAACATTTACTCGAGTAAATGTTGAGCTTGGTGAAC 2424 chr19 ENST00000247005.7 GDF1 AATTCAAAAAGAGTTCACCAAGCTCAACATTCTCGAGAATGTTGAGCTTGGTGAACTC 2425 chr19 ENST00000247005.7 GDF1 AATTCAAAAACCCTTATGAACCTCTACTGGTCTCGAGACCAGTAGAGGTTCATAAGGG 2426 chr19 ENST00000247005.7 GDF10 AATTCAAAAACAGGATAATCGTGGTGTAAATCTCGAGATTTACACCACGATTATCCTG 2427 chr10 ENST00000580279.1 GDF10 AATTCAAAAACGACCAGAAGGCCGTGTATTTCTCGAGAAATACACGGCCTTCTGGTCG 2428 chr10 ENST00000580279.1 GDF10 AATTCAAAAACTGTCCGCCAGTGCATCATTACTCGAGTAATGATGCACTGGCGGACAG 2429 chr10 ENST00000580279.1 GDF11 AATTCAAAAACCTGCAGATCTTGCGACTAAACTCGAGTTTAGTCGCAAGATCTGCAGG 2430 chr12 ENST00000257868.9 GDF11 AATTCAAAAAGATCGCTGTGGCTGCTCTTAACTCGAGTTAAGAGCAGCCACAGCGATC 2431 chr12 ENST00000257868.9 GDF11 AATTCAAAAAGAGATGTAGAGACAGTGATAGCTCGAGCTATCACTGTCTCTACATCTC 2432 chr12 ENST00000257868.9 GDF15 AATTCAAAAAAGACTCCAGATTCCGAGAGTTCTCGAGAACTCTCGGAATCTGGAGTCT 2433 chr19 ENST00000252809.3 GDF15 AATTCAAAAAGCTCCAGACCTATGATGACTTCTCGAGAAGTCATCATAGGTCTGGAGC 2434 chr19 ENST00000252809.3 GDF15 AATTCAAAAAAGAGCTGGGAAGATTCGAACACTCGAGTGTTCGAATCTTCCCAGCTCT 2435 chr19 ENST00000252809.3 GDF2 AATTCAAAAACAACAGGTACACGTCCGATAACTCGAGTTATCGGACGTGTACCTGTTG 2436 chr10 ENST00000581492.2 GDF2 AATTCAAAAATGAAAGGAAGCGTGGTCATTTCTCGAGAAATGACCACGCTTCCTTTCA 2437 chr10 ENST00000581492.2 GDF2 AATTCAAAAATATGAAGCCTACGAGTGTAAGCTCGAGCTTACACTCGTAGGCTTCATA 2438 chr10 ENST00000581492.2 GDF3 AATTCAAAAAACCGTCACCAGCTATTCATTACTCGAGTAATGAATAGCTGGTGACGGT 2439 chr12 ENST00000329913.3 GDF3 AATTCAAAAACTCTCAACAGCTCCAATTATGCTCGAGCATAATTGGAGCTGTTGAGAG 2440 chr12 ENST00000329913.3 GDF3 AATTCAAAAATTGGGCCAGGCAGTCCAATTTCTCGAGAAATTGGACTGCCTGGCCCAA 2441 chr12 ENST00000329913.3 GDF5 AATTCAAAAACAACACCATCACCAGCTTTATCTCGAGATAAAGCTGGTGATGGTGTTG 2442 chr20 ENST00000374369.7 GDF5 AATTCAAAAAATGAGACTCAGCCCACCATTTCTCGAGAAATGGTGGGCTGAGTCTCAT 2443 chr20 ENST00000374369.7 GDF5 AATTCAAAAATGAGTGTGACTTGGGCTAAAGCTCGAGCTTTAGCCCAAGTCACACTCA 2444 chr20 ENST00000374369.7 GDF6 AATTCAAAAAGACTCCCATCAGCATTCTATACTCGAGTATAGAATGCTGATGGGAGTC 2445 chr8 ENST00000287020.6 GDF6 AATTCAAAAACGAGTACATGCTGTCAATCTACTCGAGTAGATTGACAGCATGTACTCG 2446 chr8 ENST00000287020.6 GDF6 AATTCAAAAACAGTCTTCCAAGTCGGCTAATCTCGAGATTAGCCGACTTGGAAGACTG 2447 chr8 ENST00000287020.6 GDF7 AATTCAAAAAGCAGAGGAAAGAGAGCTTATTCTCGAGAATAAGCTCTCTTTCCTCTGC 2448 chr2 ENST00000272224.4 GDF7 AATTCAAAAAGTTCGACGTGTCCAGCCTTAACTCGAGTTAAGGCTGGACACGTCGAAC 2449 chr2 ENST00000272224.4 GDF7 AATTCAAAAACCACTTCATGATGTCGCTTTACTCGAGTAAAGCGACATCATGAAGTGG 2450 chr2 ENST00000272224.4 GDF9 AATTCAAAAAGATGGCTCAATTGCCTATAAACTCGAGTTTATAGGCAATTGAGCCATC 2451 chr5 ENST00000378673.2 GDF9 AATTCAAAAACCATCAGTGGAACTGCTATTTCTCGAGAAATAGCAGTTCCACTGATGG 2452 chr5 ENST00000378673.2 GDF9 AATTCAAAAAGAGTGAATACTTCAGACAATTCTCGAGAATTGTCTGAAGTATTCACTC 2453 chr5 ENST00000378673.2 GPI AATTCAAAAACGTCTGGTATGTCTCCAACATCTCGAGATGTTGGAGACATACCAGACG 2454 chr19 ENST00000356487.9 GPI AATTCAAAAACGTCTGGTATGTCTCCAACATCTCGAGATGTTGGAGACATACCAGACG 2455 chr19 ENST00000356487.9 GPI AATTCAAAAAGCGGATGTTCAATGGTGAGAACTCGAGTTCTCACCATTGAACATCCGC 2456 chr19 ENST00000356487.9 GREM1 AATTCAAAAAGCAGTGTCGTTGCATATCCATCTCGAGATGGATATGCAACGACACTGC 2457 chr15 ENST00000622074.1 GREM1 AATTCAAAAAACAGCCACCTACCAAGAAGAACTCGAGTTCTTCTTGGTAGGTGGCTGT 2458 chr15 ENST00000622074.1 GREM1 AATTCAAAAACAACAGTCGCACCATCATCAACTCGAGTTGATGATGGTGCGACTGTTG 2459 chr15 ENST00000622074.1 GREM2 AATTCAAAAAGCTGTGAAGGAAGGAAATTTACTCGAGTAAATTTCCTTCCTTCACAGC 2460 chr1 ENST00000318160.4 GREM2 AATTCAAAAACAAGGTGCATTTCTGTCATTTCTCGAGAAATGACAGAAATGCACCTTG 2461 chr1 ENST00000318160.4 GREM2 AATTCAAAAACGGAAGTAGACGTAACTTATTCTCGAGAATAAGTTACGTCTACTTCCG 2462 chr1 ENST00000318160.4 GRN AATTCAAAAAGCCCTGATAGTCAGTTCGAATCTCGAGATTCGAACTGACTATCAGGGC 2463 chr17 ENST00000053867.7 GRN AATTCAAAAAGCCCTGATAGTCAGTTCGAATCTCGAGATTCGAACTGACTATCAGGGC 2464 chr17 ENST00000053867.7 GRN AATTCAAAAACTTCCAAAGATCAGGTAACAACTCGAGTTGTTACCTGATCTTTGGAAG 2465 chr17 ENST00000053867.7 HAX1 AATTCAAAAAACAGACACTTCGGGACTCAATCTCGAGATTGAGTCCCGAAGTGTCTGT 2466 chr1 ENST00000328703.11 HAX1 AATTCAAAAACCAGCCCAAATCCTATTTCAACPCGAGTTGAAATAGGATTTGGGCTGG 2467 chr1 ENST00000328703.11 HAX1 AATTCAAAAACCAGAGGCCATTTCATAGGTTCTCGAGAACCTATGAAATGGCCTCTGG 2468 chr1 ENST00000328703.11 HFE2 AATTCAAAAAGACATGATCATTAGCCATAAGCTCGAGCTTATGGCTAATGATCATGTC 2469 chr1 ENST00000336751.10 HFE2 AATTCAAAAAGCCTACATTGGCACAACTATACTCGAGTATAGTTGTGCCAATGTAGGC 2470 chr1 ENST00000336751.10 HFE2 AATTCAAAAAGAAGCTCACCATCATATTTAACTCGAGTTAAATATGATGGTGAGCTTC 2471 chr1 ENST00000336751.10 HMGB1 AATTCAAAAAGATGCAGCTTATACGAAATAACTCGAGTTATTTCGTATAAGCTGCATC 2472 chr13 ENST00000339872.8 HMGB1 AATTCAAAAAGTTGGTGCACAGCACAAATTACTCGAGTAATTTGTGCTGTGCACCAAC 2473 chr13 ENST00000339872.8 HMGB1 AATTCAAAAAAGAAGATGATGATGATGAATACTCGAGTATTCATCATCATCATCTTCT 2474 chr13 ENST00000339872.8 HYAL2 AATTCAAAAACCTGCCAGTACCTCAAAGATTCTCGAGAATCTTTGAGGTACTGGCAGG 2475 chr3 ENST00000357750.8 HYAL2 AATTCAAAAACCTGCCAGTACCTCAAAGATTCTCGAGAATCTTTGAGGTACTGGCAGG 2476 chr3 ENST00000357750.8 HYAL2 AATTCAAAAACTGGACCTGAATGCCTTTGATCTCGAGATCAAAGGCATTCAGGTCCAG 2477 chr3 ENST00000357750.8 ICAM3 AATTCAAAAAGTCCAGCTCACGAGGCAAATACTCGAGTATTTGCCTCGTGAGCTGGAC 2478 chr19 ENST00000160262.9 ICAM3 AATTCAAAAACCAGCTCAACTTCAGCTAAATCTCGAGATTTAGCTGAAGTTGAGCTGG 2479 chr19 ENST00000160262.9 ICAM3 AATTCAAAAAGCACTTGAAATGGAAAGATAACTCGAGTTATCTTTCCATTTCAAGTGC 2480 chr19 ENST00000I60262.9 ICAM3 AATTCAAAAAGAGCGGCAGTTACCATGTTAGCTCGAGCTAACATGGTAACTGCCGCTC 2481 chr19 ENST00000160262.9 ICOS AATTCAAAAAGCACGACCCTAACGGTGAATACTCGAGTATTCACCGTTAGGGTCGTGC 2482 ch2 ENST00000316386.10 ICOS AATTCAAAAAGTCCGCATTTCACTATCATACCTCGAGGTATGATAGTGAAATGCGGAC 2483 ch2 ENST00000316386.10 ICOS AATTCAAAAACCATTCTCATGCCAACTATTACTCGAGTAATAGTTGGCATGAGAATGG 2484 ch2 ENST00000316386.10 ICOS AATTCAAAAACACAGATGTGACCCTATAATACTCGAGTATTATAGGGTCACATCTGTG 2485 ch2 ENST00000316386.10 IFNA10 AATTCAAAAATGTAAAGAAGTGTCGTGTATACTCGAGTATACACGACACTTCTTTACA 2486 chr9 ENST00000357374.2 IFNA10 AATTCAAAAAATAACCACGACGCGTTGAATCCTCGAGGATTCAACGCGTCGTGGTTAT 2487 chr9 ENST00000357374.2 IFNA10 AATTCAAAAACCTGGGACAAATGGGAAGAATCTCGAGATTCTTCCCATTTGTCCCAGG 2488 chr9 ENST00000357374.2 IFNA14 AATTCAAAAACTGGGCTGTAATCTGTCTCAACTCGAGTTGAGACAGATTACAGCCCAG 2489 chr9 ENST00000380222.3 IFNA14 AATTCAAAAACCTGAATAACAGGAGGACTTTCTCGAGAAAGTCCTCCTGTTATTCAGG 2490 chr9 ENST00000380222.3 IFNA14 AATTCAAAAAGCAGCAGACCTTCAATCTCTTCTCGAGAAGAGATTGAAGGTCTGCTGC 2491 chr9 ENST00000380222.3 IFNA16 AATTCAAAAATGTAAAGAAGCATCGTGTTTACTCGAGTAAACACGATGCTTCTTTACA 2492 chr9 ENST00000380216.1 IFNA16 AATTCAAAAAATGATCCTCATTGATTAATACCTCGAGGTATTAATCAATGAGGATCAT 2493 chr9 ENST00000380216.1 IFNA16 AATTCAAAAACCTGAAGGACAGATATGATTTCTCGAGAAATCATATCTGTCCTTCAGG 2494 chr9 ENST00000380216.1 IFNA2 AATTCAAAAAGCACAGTGGTTAATGTAATAACTCGAGTTATTACATTAACCACTGTGC 2495 chr9 ENST00000380206.3 IFNA2 AATTCAAAAATATGACCATGACACGATTTAACTCGAGTTAAATCGTGTCATGGTCATA 2496 chr9 ENST00000380206.3 IFNA2 AATTCAAAAACCATGCTGACTGATCCATTATCTCGAGATAATGGATCAGTCAGCATGG 2497 chr9 ENST00000380206.3 IFNA5 AATTCAAAAAACTTGGGATGAGACACTTCTACTCGAGTAGAAGTGTCTCATCCCAAGT 2498 chr9 ENST00000610521.1 IFNA5 AATTCAAAAAAGTGGAAGACACTCCTCTGATCTCGAGATCAGAGGAGTGTCTTCCACT 2499 chr9 ENST00000610521.1 IFNA5 AATTCAAAAATCAACTGCAAGTCAATCTGTTCTCGAGAACAGATTGACTTGCAGTTGA 2500 chr9 ENST00000610521.1 IFNA6 AATTCAAAAAGACAGACATGACTTCAGATTTCTCGAGAAATCTGAAGTCATGTCTGTC 2501 chr9 ENST00000380210.1 IFNA6 AATTCAAAAACTGTCCTCCATGAGGTGATTCCTCGAGGAATCACCTCATGGAGGACAG 2502 chr9 ENST00000380210.1 IFNA6 AATTCAAAAAAGGCTTCTAGACAAACTCTATCTCGAGATAGAGTTTGTCTAGAAGCCT 2503 chr9 ENST00000380210.1 IFNA8 AATTCAAAAATAACTATCTATAGGGCTTAAACTCGAGTTTAAGCCCTATAGATAGTTA 2504 chr9 ENST00000380205.1 IFNA8 AATTCAAAAACCAGGAGGAGTTTGATGATAACTCGAGTTATCATCAAACTCCTCCTGG 2505 chr9 ENST00000380205.1 IFNA8 AATTCAAAAAGACCTGGTACAACACGGAAATCTCGAGATTTCCGTGTTGTACCAGGTC 2506 chr9 ENST00000380205.1 IFNAR1 AATTCAAAAAGCCAAGATTCAGGAAATTATTCTCGAGAATAATTTCCTGAATCTTGGC 2507 chr21 ENST00000270139.7 IFNAR1 AATTCAAAAAGCTCTCCCGTTTGTCATTTATCTCGAGATAAATGACAAACGGGAGAGC 2508 chr21 ENST00000270139.7 IFNAR1 AATTCAAAAAATGAACTGTGTCAAGTATAAGCTCGAGCTTATACTTGACACAGTTCAT 2509 chr21 ENST00000270139.7 IFNAR2 AATTCAAAAAGAGTGGAAATTTCACCTATATCTCGAGATATAGGTGAAATTTCCACTC 2510 chr21 ENST00000342136.8 IFNAR2 AATTCAAAAATGTATATCAGCCTCGTGTTTGCTCGAGCAAACACGAGGCTGATATACA 2511 chr21 ENST00000342136.8 IFNAR2 AATTCAAAAAGCAAATACCACAAGATCATTTCTCGAGAAATGATCTTGTGGTATTTGC 2512 chr21 ENST00000342136.8 IFNB1 AATTCAAAAAATTGAATGGGAGGCTTGAATACTCGAGTATTCAAGCCTCCCATTCAAT 2513 chr9 ENST00000380232.3 IFNB1 AATTCAAAAACCTACAAAGAAGCAGCAATTTCTCGAGAAATTGCTGCTTCTTTGTAGG 2514 chr9 ENST00000380232.3 IFNB1 AATTCAAAAACTAATGTCTATCATCAGATAACTCGAGTTATCTGATGATAGACATTAG 2515 chr9 ENST00000380232.3 IFNE AATTCAAAAAGGTAGTGATAACCTTAGATTACTCGAGTAATCTAAGGTTATCACTACC 2516 chr9 ENST00000448696.4 IFNE AATTCAAAAAAGCCTCTTCAGGGCAAATATTCTCGAGAATATTTGCCCTGAAGAGGCT 2517 chr9 ENST00000448696.4 IFNE AATTCAAAAACATAGAGTGGTAATACAATTTCTCGAGAAATTGTATTACCACTCTATG 2518 chr9 ENST00000448696.4 IFNG AATTCAAAAAGGTTGTCCTGCCTGCAATATTCTCGAGAATATTGCAGGCAGGACAACC 2519 chr12 ENST00000229135.3 IFNG AATTCAAAAACATTCAGATGTAGCGGATAATCTCGAGATTATCCGCTACATCTGAATG 2520 chr12 ENST00000229135.3 IFNG AATTCAAAAATGTTACTGCCAGGACCCATATCTCGAGATATGGGTCCTGGCAGTAACA 2521 chr12 ENST00000229135.3 IFNGR1 AATTCAAAAAACGAGCAGGAAGTCGATTATGCTCGAGCATAATCGACTTCCTGCTCGT 2522 chr6 ENST00000367739.8 IFNGR1 AATTCAAAAACATGAACCCTATCGTATATTGCTCGAGCAATATACGATAGGGTTCATG 2523 chr6 ENST00000367739.8 IFNGR1 AATTCAAAAACGGAAGTGAGATCCAGTATAACTCGAGTTATACTGGATCTCACTTCCG 2524 chr6 ENST00000367739.8 IFNK AATTCAAAAAGAGATTGTGGCTACGCAAATGCTCGAGCATTTGCGTAGCCACAATCTC 2525 chr9 ENST00000276943.2 IFNK AATTCAAAAACTGTTCAGATTCAAGATTATTCTCGAGAATAATCTTGAATCTGAACAG 2526 chr9 ENST00000276943.2 IFNK AATTCAAAAATCAGCCAACACACCTTCAAATCTCGAGATTTGAAGGTGTGTTGGCTGA 2527 chr9 ENST00000276943.2 IFNL1 AATTCAAAAACTCACGCGAGACCTCAAATATCTCGAGATATTTGAGGTCTCGCGTGAG 2528 chr19 ENST00000333625.2 IFNL1 AATTCAAAAAGCCACATTGGCAGGTTCAAATCTCGAGATTTGAACCTGCCAATGTGGC 2529 chr19 ENST00000333625.2 IFNL1 AATTCAAAAAGAGTTGCAGCTCTCCTGTCTTCTCGAGAAGACAGGAGAGCTGCAACTC 2530 chr19 ENST00000333625.2 IFNL3 AATTCAAAAAAGGGCCAAAGATGCCTTAGAACTCGAGTTCTAAGGCATCTTTGGCCCT 2531 chr19 ENST00000413851.2 IFNL3 AATTCAAAAAGCCTTTAAGAGGGCCAAAGATCTCGAGATCTTTGGCCCTCTTAAAGGC 2532 chr19 ENST00000413851.2 IFNL3 AATTCAAAAATGCCACATAGCCCAGTTCAAGCTCGAGCTTGAACTGGGCTATGTGGCA 2533 chr19 ENST00000413851.2 IFNW1 AATTCAAAAAAGACTCTTATTTCGGCTTTAACTCGAGTTAAAGCCGAAATAAGAGTCT 2534 chr9 ENST00000380229.3 IFNW1 AATTCAAAAATCAGTCCCTAAGATGTTATTTCTCGAGAAATAACATCTTAGGGACTGA 2535 chr9 ENST00000380229.3 IFNW1 AATTCAAAAACGGTATATTAAGCCAGTATATCTCGAGATATACTGGCTTAATATACCG 2536 chr9 ENST00000380229.3 IL10 AATTCAAAAAAGCTTCTCTGTGAACGATTTACTCGAGTAAATCGTTCACAGAGAAGCT 2537 chr1 ENST00000423557.1 IL10 AATTCAAAAAGCAGGTGAAGAATGCCTTTAACTCGAGTTAAAGGCATTCTTCACCTGC 2538 chr1 ENST00000423557.1 IL10 AATTCAAAAAGCTGGACAACTTGTTGTTAAACTCGAGTTTAACAACAAGTTGTCCAGC 2539 chr1 ENST00000423557.1 IL10RA AATTCAAAAATCTGTCGCTTCCCGAAGTAACCTCGAGGTTACTTCGGGAAGCGACAGA 2540 chr11 ENST00000227752.7 IL10RA AATTCAAAAAGAAACAGGATCCTCTAGAAATCTCGAGATTTCTAGAGGATCCTGTTTC 2541 chr11 ENST00000227752.7 IL10RA AATTCAAAAAGAACTCTTTCCTGTATCATAACTCGAGTTATGATACAGGAAAGAGTTC 2542 chr11 ENST00000227752.7 IL11 AATTCAAAAAATATCCACTTGAGGGCGATTTCTCGAGAAATCGCCCTCAAGTGGATAT 2543 chr19 ENST00000264563.6 IL11 AATTCAAAAACCTTCCAAAGCCAGATCTTATCTCGAGATAAGATCTGGCTTTGGAAGG 2544 chr19 ENST00000264563.6 IL11 AATTCAAAAATGCACAGCTGAGGGACAAATTCTCGAGAATTTGTCCCTCAGCTGTGCA 2545 chr19 ENST00000264563.6 IL11RA AATTCAAAAACGGCAGATTCCACCTATAATTCTCGAGAATTATAGGTGGAATCTGCCG 2546 chr9 ENST00000318041.13 IL11RA AATTCAAAAATCGGCAGATTCCACCTATAATCTCGAGATTATAGGTGGAATCTGCCGA 2547 chr9 ENST00000318041.13 IL11RA AATTCAAAAATGGAGCCAGTACCGGATTAATCTCGAGATTAATCCGGTACTGGCTCCA 2548 chr9 ENST00000318041.13 IL12A AATTCAAAAATGATACCTCTGATCAAGTATTCTCGAGAATACTTGATCAGAGGTATCA 2549 chr3 ENST00000305579.6 IL12A AATTCAAAAACCTGTGCCTTAGTAGTATTTACTCGAGTAAATACTACTAAGGCACAGG 2550 chr3 ENST00000305579.6 IL12A AATTCAAAAACCTGTTTACCATTGGAATTAACTCGAGTTAATTCCAATGGTAAACAGG 2551 chr3 ENST00000305579.6 IL12B AATTCAAAAAGAATTTGGTCCACTGATATTTCTCGAGAAATATCAGTGGACCAAATTC 2552 chr5 ENST00000231228.2 IL12B AATTCAAAAACCATGGGCCTTCATGCTATTTCTCGAGAAATAGCATGAAGGCCCATGG 2553 chr5 ENST00000231228.2 IL12B AATTCAAAAATTAGATGCTAAATGCTCATTGCTCGAGCAATGAGCATTTAGCATCTAA 2554 chr5 ENST00000231228.2 IL12RB1 AATTCAAAAACAGCTCTACAACTCAGTTAAACTCGAGTTTAACTGAGTTGTAGAGCTG 2555 chr19 ENST00000593993.6 IL12RB1 AATTCAAAAAGTCATCTCCTCGAACCAATTTCTCGAGAAATTGGTTCGAGGAGATGAC 2556 chr19 ENST00000593993.6 IL12RB1 AATTCAAAAACCAACGGGACCACCATGTATTCTCGAGAATACATGGTGGTCCCGTTGG 2557 chr19 ENST00000593993.6 IL13 AATTCAAAAAACTTCGAAAGCATCATTATTTCTCGAGAAATAATGATGCTTTCGAAGT 2558 chr5 ENST00000304506.7 IL13 AATTCAAAAAATTGAAGTTGCAGATTCATTTCTCGAGAAATGAATCTGCAACTTCAAT 2559 chr5 ENST00000304506.7 IL13 AATTCAAAAACCTGCTCTTACATTTAAAGAACTCGAGTTCTTTAAATGTAAGAGCAGG 2560 chr5 ENST00000304506.7 IL15 AATTCAAAAAGAAGATCTTATTCAATCTATGCTCGAGCATAGATTGAATAAGATCTTC 2561 chr4 ENST00000296545.11 IL15 AATTCAAAAATAAGGGTGATAGTCAAATTATCTCGAGATAATTTGACTATCACCCTTA 2562 chr4 ENST00000296545.11 IL15 AATTCAAAAACACTCTGCTGCTTAGACATAACTCGAGTTATGTCTAAGCAGCAGAGTG 2563 chr4 ENST00000296545.11 IL16 AATTCAAAAATGGGACCACGTGAGATCATTCCTCGAGGAATGATCTCACGTGGTCCCA 2564 chr15 ENST00000302987.8 IL16 AATTCAAAAAGTTCTGGATGAAGCAACATTACTCGAGTAATGTTGCTTCATCCAGAAC 2565 chr15 ENST00000302987.8 IL16 AATTCAAAAACCCAAACAGTGACATTTATTTCTCGAGAAATAAATGTCACTGTTTGGG 2566 chr15 ENST00000302987.8 IL17A AATTCAAAAAATCAGTTCTGCCTAGGTAAATCTCGAGATTTACCTAGGCAGAACTGAT 2567 chr6 ENST00000340057.1 IL17A AATTCAAAAAGAGCTATTTAAGGATCTATTTCTCGAGAAATAGATCCTTAAATAGCTC 2568 chr6 ENST00000340057.1 IL17A AATTCAAAAAGGTCAACCTGAACATCCATAACTCGAGTTATGGATGTTCAGGTTGACC 2569 chr6 ENST00000340057.1 IL17B AATTCAAAAATATGCCCGCATGGAGGAGTATCTCGAGATACTCCTCCATGCGGGCATA 2570 chr5 ENST00000261796.3 IL17B AATTCAAAAAGTGTCACGGATGAAACCGTATCTCGAGATACGGTTTCATCCGTGACAC 2571 chr5 ENST00000261796.3 IL17B AATTCAAAAAGCAGCTGTGGATGTCCAACAACTCGAGTTGTTGGACATCCACAGCTGC 2572 chr5 ENST00000261796.3 IL17C AATTCAAAAAGCACCTCTTCCAGCCCTTAAACTCGAGTTTAAGGGCTGGAAGAGGTGC 2573 chr16 ENST00000244241.4 IL17C AATTCAAAAACTTTGCCTTCCACACCGAGTTCTCGAGAACTCGGTGTGGAAGGCAAAG 2574 chr16 ENST00000244241.4 IL17C AATTCAAAAAATCTCCAGCCTCAGTAGTTGGCTCGAGCCAACTACTGAGGCTGGAGAT 2575 chr16 ENST00000244241.4 IL17D AATTCAAAAAAGAGCTACTCTGTTACATTTCCTCGAGGAAATGTAACAGAGTAGCTCT 2576 chr13 ENST00000304920.3 IL17D AATTCAAAAACAAAGAGATAGGGACGCATATCTCGAGATATGCGTCCCTATCTCTTTG 2577 chr13 ENST00000304920.3 IL17D AATTCAAAAAAGACAGCATCAACTCCAGCATCTCGAGATGCTGGAGTTGATGCTGTCT 2578 chr13 ENST00000304920.3 IL17F AATTCAAAAATCATCCACCATGTGCAGTAAGCTCGAGCTTACTGCACATGGTGGATGA 2579 chr6 ENST00000336123.4 IL17F AATTCAAAAAGTACTTGCTGCTGTCGATATTCTCGAGAATATCGACAGCAGCAAGTAC 2580 chr6 ENST00000336123.4 IL17F AATTCAAAAACGTTTCCATGTCACGTAACATCTCGAGATGTTACGTGACATGGAAACG 2581 chr6 ENST00000336123.4 IL18 AATTCAAAAACCCGGACCATATTTATTATAACTCGAGTTATAATAAATATGGTCCGGG 2582 chr11 ENST00000280357.11 IL18 AATTCAAAAATGATTCTGACTGTAGAGATAACTCGAGTTATCTCTACAGTCAGAATCA 2583 chr11 ENST00000280357.11 IL18 AATTCAAAAATGGCAAGCTTGAATCTAAATTCTCGAGAATTTAGATTCAAGCTTGCCA 2584 chr11 ENST00000280357.11 IL18BP AATTCAAAAAGGTCCCTTCTCTCACCAAATTCTCGAGAATTTGGTGAGAGAAGGGACC 2585 chr11 ENST00000260049.9 IL18BP AATTCAAAAATCCCATGTCTCTGCTCATTTACTCGAGTAAATGAGCAGAGACATGGGA 2586 chr11 ENST00000260049.9 IL18BP AATTCAAAAACTGGGCAATGGTTCCTTCATTCTCGAGAATGAAGGAACCATTGCCCAG 2587 chr11 ENST00000260049.9 IL19 AATTCAAAAAGTCCACGCTGCTGCCATTAAACTCGAGTTTAATGGCAGCAGCGTGGAC 2588 chr1 ENST00000270218.10 IL19 AATTCAAAAATCCACAGACATGCACCATATACTCGAGTATATGGTGCATGTCTGTGGA 2589 chr1 ENST00000270218.10 IL19 AATTCAAAAATGATGACAAGGAACCTGTATACTCGAGTATACAGGTTCCTTGTCATCA 2590 chr1 ENST00000270218.10 IL1A AATTCAAAAAGTGGAACCAACACTAACATATCTCGAGATATGTTAGTGTTGGTTCCAC 2591 chr2 ENST00000263339.3 IL1A AATTCAAAAAGCCCTCAATCAAAGTATAATTCTCGAGAATTATACTTTGATTGAGGGC 2592 chr2 ENST00000263339.3 IL1A AATTCAAAAATATTACAGATGGGCAAATTAACTCGAGTTAATTTGCCCATCTGTAATA 2593 chr2 ENST00000263339.3 IL1B AATTCAAAAAATCAATAACAAGCTGGAATTTCTCGAGAAATTCCAGCTTGTTATTGAT 2594 chr2 ENST00000263341.6 IL1B AATTCAAAAAAGCAACCGCTTCCCTATTTATCTCGAGATAAATAGGGAAGCGGTTGCT 2595 chr2 ENST00000263341.6 IL1B AATTCAAAAACTGACTTCACCATGCAATTTGCTCGAGCAAATTGCATGGTGAAGTCAG 2596 chr2 ENST00000263341.6 IL1F10 AATTCAAAAATCCTTGTGGGCTCAGTTTAATCTCGAGATTAAACTGAGCCCACAAGGA 2597 chr2 ENST00000341010.6 IL1F10 AATTCAAAAAGGTCTATGGTAGGCAGAATAACTCGAGTTATTCTGCCTACCATAGACC 2598 chr2 ENST00000341010.6 IL1F10 AATTCAAAAATGCAGACCAGAAGGCTCTATACTCGAGTATAGAGCCTTCTGGTCTGCA 2599 chr2 ENST00000341010.6 IL1R1 AATTCAAAAAGCCAAGAATACACATGGTATACTCGAGTATACCATGTGTATTCTTGGC 2600 chr2 ENST00000410023.5 IL1R1 AATTCAAAAAATAATGCACAAGCCATATTTACTCGAGTAAATATGGCTTGTGCATTAT 2601 chr2 ENST00000410023.5 IL1R1 AATTCAAAAATGGTATAGATGCAGCATATATCTCGAGATATATGCTGCATCTATACCA 2602 chr2 ENST00000410023.5 IL1R2 AATTCAAAAACAATCCCGTGTAAGGTGTTTCCTCGAGGAAACACCTTACACGGGATTG 2603 chr2 ENST00000332549.7 IL1R2 AATTCAAAAAGACCATTCCTGTGATCATTTCCTCGAGGAAATGATCACAGGAATGGTC 2604 chr2 ENST00000332549.7 IL1R2 AATTCAAAAACGTTCATCTCATACCCGCAAACTCGAGTTTGCGGGTATGAGATGAACG 2605 chr2 ENST00000332549.7 IL1RAPL1 AATTCAAAAACAAAGCAAGCGGCTGATTATTCTCGAGAATAATCAGCCGCTTGCTTTG 2606 chrX ENST00000378993.5 IL1RAPL1 AATTCAAAAAGCCAGCGTTCTCCTTCATAAACTCGAGTTTATGAAGGAGAACGCTGGC 2607 chrX ENST00000378993.5 IL1RAPL1 AATTCAAAAATCAAGCTCCTGACGGTCATTACTCGAGTAATGACCGTCAGGAGCTTGA 2608 chrX ENST00000378993.5 IL1RL1 AATTCAAAAATTACACCGTGGATTGGTATTACTCGAGTAATACCAATCCACGGTGTAA 2609 chr2 ENST00000233954.5 IL1RL1 AATTCAAAAAAGTTGCTGATTCTGGTATTTACTCGAGTAAATACCAGAATCAGCAACT 2610 chr2 ENST00000233954.5 IL1RL1 AATTCAAAAACGTGAAGGAAGAGGATTTATTCTCGAGAATAAATCCTCTTCCTTCACG 2611 chr2 ENST00000233954.5 IL1RN AATTCAAAAAGCAAGGACCAAATGTCAATTTCTCGAGAAATTGACATTTGGTCCTTGC 2612 chr2 ENST00000409930.3 IL1RN AATTCAAAAACGTCATGGTCACCAAATTCTACTCGAGTAGAATTTGGTGACCATGACG 2613 chr2 ENST00000409930.3 IL1RN AATTCAAAAACTGCCTCCAGAATGGTCTTTCCTCGAGGAAAGACCATTCTGGAGGCAG 2614 chr2 ENST00000409930.3 IL2 AATTCAAAAAGCTACCTATTGTAACTATTATCTCGAGATAATAGTTACAATAGGTAGC 2615 chr4 ENST00000226730.4 IL2 AATTCAAAAACAGCTACAACTGGAGCATTTACTCGAGTAAATGCTCCAGTTGTAGCTG 2616 chr4 ENST00000226730.4 IL2 AATTCAAAAATGCTGGATTTACAGATGATTTCTCGAGAAATCATCTGTAAATCCAGCA 2617 chr4 ENST00000226730.4 IL20 AATTCAAAAACTGATGCTCTGTGAGATATTTCTCGAGAAATATCTCACAGAGCATCAG 2618 chr1 ENST00000367096.7 IL20 AATTCAAAAATGGTCACAGTGTATCTTATTTCTCGAGAAATAAGATACACTGTGACCA 2619 chr1 ENST00000367096.7 IL20 AATTCAAAAAGGACTGAAGACACTCAATTTGCTCGAGCAAATTGAGTGTCTTCAGTCC 2620 chr1 ENST00000367096.7 IL20RA AATTCAAAAACCAGTATTATGCCAAAGTTAACTCGAGTTAACTTTGGCATAATACTGG 2621 chr6 ENST00000316649.9 IL20RA AATTCAAAAAGAGGGTCTTCAAGGAGTTAAACTCGAGTTTAACTCCTTGAAGACCCTC 2622 chr6 ENST00000316649.9 IL20RA AATTCAAAAAGCTTCGCATTTGATGGAAATTCTCGAGAATTTCCATCAAATGCGAAGC 2623 chr6 ENST00000316649.9 IL20RB AATTCAAAAACAGTGTACTATTCTGTCGAATCTCGAGATTCGACAGAATAGTACACTG 2624 chr3 ENST00000329582.8 IL20RB AATTCAAAAACCAGAATAATCCTTGAGAGAACTCGAGTTCTCTCAAGGATTATTCTGG 2625 chr3 ENST00000329582.8 IL20RB AATTCAAAAACTCTGTACTCTCAACCAACATCTCGAGATGTTGGTTGAGAGTACAGAG 2626 chr3 ENST00000329582.8 IL21 AATTCAAAAAAGGAAACCACCTTCCACAAATCTCGAGATTTGTGGAAGGTGGTTTCCT 2627 chr4 ENST00000264497.7 IL21 AATTCAAAAAATGACTTGGTCCCTGAATTTCCTCGAGGAAATTCAGGGACCAAGTCAT 2628 chr4 ENST00000264497.7 IL21 AATTCAAAAACTTTCAGAAGGCCCAACTAAACTCGAGTTTAGTTGGGCCTTCTGAAAG 2629 chr4 ENST00000264497.7 IL22 AATTCAAAAAAGGCTAAGCACATGTCATATTCTCGAGAATATGACATGTGCTTAGCCT 2630 chr12 ENST00000328087.5 IL22 AATTCAAAAAGTTTCCATAATCAGTACTTTACTCGAGTAAAGTACTGATTATGGAAAC 2631 chr12 ENST00000328087.5 IL22 AATTCAAAAAAGACTTTCTAAGCATAGATATCTCGAGATATCTATGCTTAGAAAGTCT 2632 chr12 ENST00000328087.5 IL22RA1 AATTCAAAAAGGACACTTTCTAGTCCTAAACCTCGAGGTTTAGGACTAGAAAGTGTCC 2633 chr1 ENST00000270800.1 IL22RA1 AATTCAAAAAAGGGACACCACAGTACCTAAACTCGAGTTTAGGTACTGTGGTGTCCCT 2634 chr1 ENST00000270800.1 IL22RA1 AATTCAAAAACTGTCCGAGATCACCTACTTACTCGAGTAAGTAGGTGATCTCGGACAG 2635 chr1 ENST00000270800.1 IL22RA2 AATTCAAAAAAGACATACAGGAACCTTATTACTCGAGTAATAAGGTTCCTGTATGTCT 2636 chr6 ENST00000349184.8 IL22RA2 AATTCAAAAACTCGTGTTTGAAGGATCTTATCTCGAGATAAGATCCTTCAAACACGAG 2637 chr6 ENST00000349184.8 IL22RA2 AATTCAAAAATGCTCCAAATTTACCATATAGCTCGAGCTATATGGTAAATTTGGAGCA 2638 chr6 ENST00000349184.8 IL23A AATTCAAAAAAGCTGCTAGGATCGGATATTTCTCGAGAAATATCCGATCCTAGCAGCT 2639 chr12 ENST00000228534.5 IL23A AATTCAAAAACTGTGAGCCAACAGGTTAATTCTCGAGAATTAACCTGTTGGCTCACAG 2640 chr12 ENST00000228534.5 IL23A AATTCAAAAAGGATCCACCAGGGTCTGATTTCTCGAGAAATCAGACCCTGGTGGATCC 2641 chr12 ENST00000228534.5 IL23R AATTCAAAAACTTTCTTTGATTGGGATATTTCTCGAGAAATATCCCAATCAAAGAAAG 2642 chr1 ENST00000347310.9 IL23R AATTCAAAAATATCTCACCTCAAGCTATATTCTCGAGAATATAGCTTGAGGTGAGATA 2643 chr1 ENST00000347310.9 IL23R AATTCAAAAACGACAATACTACAGTTGTATACTCGAGTATACAACTGTAGTATTGTCG 2644 chr1 ENST00000347310.9 IL24 AATTCAAAAACACAGGCGGTTTCTGCTATTCCTCGAGGAATAGCAGAAACCGCCTGTG 2645 chr1 ENST00000294984.6 IL24 AATTCAAAAAGTCAGGACTCTGAAGTCATTCCTCGAGGAATGACTTCAGAGTCCTGAC 2646 chr1 ENST00000294984.6 IL24 AATTCAAAAATCGGATGCTGAGAGCTGTTACCTCGAGGTAACAGCTCTCAGCATCCGA 2647 chr1 ENST00000294984.6 IL25 AATTCAAAAAACAGGCACTTTCTAGATATTTCTCGAGAAATATCTAGAAAGTGCCTGT 2648 chr14 ENST00000329715.2 IL25 AATTCAAAAACCACAACCAGACTGTCTTCTACTCGAGTAGAAGACAGTCTGGTTGTGG 2649 chr14 ENST00000329715.2 IL25 AATTCAAAAATCCTGTAGGGCCAGTGAAGATCTCGAGATCTTCACTGGCCCTACAGGA 2650 chr14 ENST00000329715.2 IL26 AATTCAAAAAAGCTGTTGACGCTCTCTATATCTCGAGATATAGAGAGCGTCAACAGCT 2651 chr12 ENST00000229134.4 IL26 AATTCAAAAAAGTACATTGTGTCAACTTAATCTCGAGATTAAGTTGACACAATGTACT 2652 chr12 ENST00000229134.4 IL26 AATTCAAAAACGATTCCAGAAGACCGCATAACTCGAGTTATGCGGTCTTCTGGAATCG 2653 chr12 ENST00000229134.4 IL27 AATTCAAAAAACTCCTTGGAGCTCGTCTTATCTCGAGATAAGACGAGCTCCAAGGAGT 2654 chr16 ENST00000356897.1 IL27 AATTCAAAAAACTTTAGGACTGGAGTCTTGGCTCGAGCCAAGACTCCAGTCCTAAAGT 2655 chr16 ENST00000356897.1 IL27 AATTCAAAAACATCATCAGCCTTGGACAAGGCTCGAGCCTTGTCCAAGGCTGATGATG 2656 chr16 ENST00000356897.1 IL2RA AATTCAAAAACCTCGTCACAACAACAGATTTCTCGAGAAATCTGTTGTTGTGACGAGG 2657 chr10 ENST00000379959.7 IL2RA AATTCAAAAAACCCTATACAACTGGACATTGCTCGAGCAATGTCCAGTTGTATAGGGT 2658 chr10 ENST00000379959.7 IL2RA AATTCAAAAAACTCGGAACACAACGAAACAACTCGAGTTGTTTCGTTGTGTTCCGAGT 2659 chr10 ENST00000379959.7 IL2RB AATTCAAAAAAGTCCCAGACCTGGTGGATTTCTCGAGAAATCCACCAGGTCTGGGACT 2660 chr22 ENST00000216223.9 IL2RB AATTCAAAAAGACCCACAGATGCAACATAAGCTCGAGCTTATGTTGCATCTGTGGGTC 2661 chr22 ENST00000216223.9 IL2RB AATTCAAAAACCAGACACCCAGTATGAGTTTCTCGAGAAACTCATACTGGGTGTCTGG 2662 chr22 ENST00000216223.9 IL2RG AATTCAAAAATCGTGTTCGGAGCCGCTTTAACTCGAGTTAAAGCGGCTCCGAACACGA 2663 chrX ENST00000374202.6 IL2RG AATTCAAAAACCAACCTCACTCTGCATTATTCTCGAGAATAATGCAGAGTGAGGTTGG 2664 chrX ENST00000374202.6 IL2RG AATTCAAAAATTGGCTCCATGGGATTGATTACTCGAGTAATCAATCCCATGGAGCCAA 2665 chrX ENST00000374202.6 IL3 AATTCAAAAATTATCCCATTGAGACTATTTACTCGAGTAAATAGTCTCAATGGGATAA 2666 chr5 ENST00000296870.2 IL3 AATTCAAAAACGGCATCAGATGAATTGTTAACTCGAGTTAACAATTCATCTGATGCCG 2667 chr5 ENST00000296870.2 IL3 AATTCAAAAAGCAATTGAGAGCATTCTTAAACTCGAGTTTAAGAATGCTCTCAATTGC 2668 chr5 ENST00000296870.2 IL31 AATTCAAAAAGCATATCTCAAGACAATCAGACTCGAGTCTGATTGTCTTGAGATATGC 2669 chr12 ENST00000377035.1 IL31 AATTCAAAAACCAAGTGATGATGTACAGAAACTCGAGTTTCTGTACATCATCACTTGG 2670 chr12 ENST00000377035.1 IL31 AATTCAAAAACCTGACTATTTCTCAACAGTTCTCGAGAACTGTTGAGAAATAGTCAGG 2671 chr12 ENST00000377035.1 IL31RA AATTCAAAAACATCAAACGAATGATTCAAATCTCGAGATTTGAATCATTCGTTTGATG 2672 chr5 ENST00000447346.6 IL31RA AATTCAAAAACGCCTGTTTCATCTGATTTAACTCGAGTTAAATCAGATGAAACAGGCG 2673 chr5 ENST00000447346.6 IL31RA AATTCAAAAATTTCCTGTGTCTACTACTATACTCGAGTATAGTAGTAGACACAGGAAA 2674 chr5 ENST00000447346.6 IL32 AATTCAAAAATGTCGCCCTGGCATCTTAATACTCGAGTATTAAGATGCCAGGGCGACA 2675 chr16 ENST00000325568.9 IL32 AATTCAAAAAAGAGCTCACTCCTCTACTTGACTCGAGTCAAGTAGAGGAGTGAGCTCT 2676 chr16 ENST00000325568.9 IL32 AATTCAAAAAAGAGCTGGAGGACGACTTCAACTCGAGTTGAAGTCGTCCTCCAGCTCT 2677 chr16 ENST00000325568.9 IL33 AATTCAAAAAGAGTGCTTTGCCTTTGGTATACTCGAGTATACCAAAGGCAAAGCACTC 2678 chr9 ENST00000381434.7 IL33 AATTCAAAAAGCACTCCAACTGTGTTTCATTCTCGAGAATGAAACACAGTTGGAGTGC 2679 chr9 ENST00000381434.7 IL33 AATTCAAAAACCTGTTACTTTAGGAGAGAAACTCGAGTTTCTCTCCTAAAGTAACAGG 2680 chr9 ENST00000381434.7 IL34 AATTCAAAAAGCCGACTTCAGTACATGAAACCTCGAGGTTTCATGTACTGAAGTCGGC 2681 chr16 ENST00000288098.6 IL34 AATTCAAAAACAGAGCCCTCATTGCAGTATGCTCGAGCATACTGCAATGAGGGCTCTG 2682 chr16 ENST00000288098.6 IL34 AATTCAAAAACCGTGTTGTCCCTCTTGAATGCTCGAGCATTCAAGAGGGACAACACGG 2683 chr16 ENST00000288098.6 IL36A AATTCAAAAACTCCAGTCACTATTGCCTTAACTCGAGTTAAGGCAATAGTGACTGGAG 2684 chr2 ENST00000259211.6 IL36A AATTCAAAAATTCAGGACCAGACGCTCATAGCTCGAGCTATGAGCGTCTGGTCCTGAA 2685 chr2 ENST00000259211.6 IL36A AATTCAAAAACTCTGCCTGATGTGTGCTAAACTCGAGTTTAGCACACATCAGGCAGAG 2686 chr2 ENST00000259211.6 IL36B AATTCAAAAAATCCTATGCTATTCGTGATTCCTCGAGGAATCACGAATAGCATAGGAT 2687 chr2 ENST00000327407.2 IL36B AATTCAAAAACCTGAGTGGAAATTCTTTAATCTCGAGATTAAAGAATTTCCACTCAGG 2688 chr2 ENST00000327407.2 IL36B AATTCAAAAATTGGACTACATAACCTGTAAACTCGAGTTTACAGGTTATGTAGTCCAA 2689 chr2 ENST00000327407.2 IL36G AATTCAAAAATGATATCATCCAGTCTTTATACTCGAGTATAAAGACTGGATGATATCA 2690 chr2 ENST00000259205.4 IL36G AATTCAAAAACAGGAGAGCTGGGTGGTATAACTCGAGTTATACCACCCAGCTCTCCTG 2691 chr2 ENST00000259205.4 IL36G AATTCAAAAAGGGAATCCAGAATCCAGAAATCTCGAGATTTCTGGATTCTGGATTCCC 2692 chr2 ENST00000259205.4 IL36RN AATTCAAAAACTCGGCATTGAAGGTGCTTTACTCGAGTAAAGCACCTTCAATGCCGAG 2693 chr2 ENST00000346807.7 IL36RN AATTCAAAAATGGTTCCCAGTTTGGATAAATCTCGAGATTTATCCAAACTGGGAACCA 2694 chr2 ENST00000346807.7 IL36RN AATTCAAAAAGGGAATCATTCCTGCTTAATGCTCGAGCATTAAGCAGGAATGATTCCC 2695 chr2 ENST00000346807.7 IL37 AATTCAAAAACTCTACTGTGACAAGGATAAACTCGAGTTTATCCTTGTCACAGTAGAG 2696 chr2 ENST00000263326.7 IL37 AATTCAAAAATGCACCTCCTGCAATTGTAATCTCGAGATTACAATTGCAGGAGGTGCA 2697 chr2 ENST00000263326.7 IL37 AATTCAAAAAGTTCACACAAAGATCTTCTTTCTCGAGAAAGAAGATCTTTGTGTGAAC 2698 chr2 ENST00000263326.7 IL4 AATTCAAAAAAGCTGATCCGATTCCTGAAACCTCGAGGTTTCAGGAATCGGATCAGCT 2699 chr5 ENST00000231449.6 IL4 AATTCAAAAACCACGGACACAAGTGCGATATCTCGAGATATCGCACTTGTGTCCGTGG 2700 chr5 ENST00000231449.6 IL4 AATTCAAAAATAGCATGTGCCGGCAACTTTGCTCGAGCAAAGTTGCCGGCACATGCTA 2701 chr5 ENST00000231449.6 IL5 AATTCAAAAAGCAAGAGTTTCTTGGTGTAATCTCGAGATTACACCAAGAAACTCTTGC 2702 chr5 ENST00000231454.5 IL5 AATTCAAAAAGGGTACTGTGGAAAGACTATTCTCGAGAATAGTCTTTCCACAGTACCC 2703 chr5 ENST00000231454.5 IL5 AATTCAAAAAGAAAGAGTCAGGCCTTAATTTCTCGAGAAATTAAGGCCTGACTCTTTC 2704 chr5 ENST00000231454.5 IL6 AATTCAAAAAATGAGCGTTAGGACACTATTTCTCGAGAAATAGTGTCCTAACGCTCAT 2705 chr7 ENST00000258743.9 IL6 AATTCAAAAAGAGTACCTCCAGAACAGATTTCTCGAGAAATCTGTTCTGGAGGTACTC 2706 chr7 ENST00000258743.9 IL6 AATTCAAAAAATGTGAAGCTGAGTTAATTTACTCGAGTAAATTAACTCAGCTTCACAT 2707 chr7 ENST00000258743.9 IL6R AATTCAAAAAGCAGGCACTTACTACTAATAACTCGAGTTATTAGTAGTAAGTGCCTGC 2708 chr1 ENST00000368485.7 IL6R AATTCAAAAATATCGGGCTGAACGGTCAAAGCTCGAGCTTTGACCGTTCAGCCCGATA 2709 chr1 ENST00000368485.7 IL6R AATTCAAAAACTGGACCCTGTGGATGATAAACTCGAGTTTATCATCCACAGGGTCCAG 2710 chr1 ENST00000368485.7 IL6ST AATTCAAAAAACCGTGCATCGCACCTATTTACTCGAGTAAATAGGTGCGATGCACGGT 2711 chr5 ENST00000336909.9 IL6ST AATTCAAAAAACTTCAGCAGTACCTATAAAGCTCGAGCTTTATAGGTACTGCTGAAGT 2712 chr5 ENST00000336909.9 IL6ST AATTCAAAAACGGCCAGAAGATCTACAATTACTCGAGTAATTGTAGATCTTCTGGCCG 2713 chr5 ENST00000336909.9 IL7 AATTCAAAAAGCTCGCAAGTTGAGGCAATTTCTCGAGAAATTGCCTCAACTTGCGAGC 2714 chr8 ENST00000263851.8 IL7 AATTCAAAAAGCTCACTATGAATCTATTATACTCGAGTATAATAGATTCATAGTGAGC 2715 chr8 ENST00000263851.8 IL7 AATTCAAAAAGTGTTTCCTAAAGAGACTATTCTCGAGAATAGTCTCTTTAGGAAACAC 2716 chr8 ENST00000263851.8 IL9 AATTCAAAAAACCACCATGCAAACAAGATACCTCGAGGTATCTTGTTTGCATGGTGGT 2717 chr5 ENST00000274520.1 IL9 AATTCAAAAAGAACAACAAGTGTCCATATTTCTCGAGAAATATGGACACTTGTTGTTC 2718 chr5 ENST00000274520.1 IL9 AATTCAAAAACTGAAGAGTCTTCTGGAAATTCTCGAGAATTTCCAGAAGACTCTTCAG 2719 chr5 ENST00000274520.1 INHA AATTCAAAAACCTCGGATGGAGGTTACTCTTCTCGAGAAGAGTAACCTCCATCCGAGG 2720 chr2 ENST00000243786.2 INHA AATTCAAAAAGCAGCACTGTGCTTGTATCTACTCGAGTAGATACAAGCACAGTGCTGC 2721 chr2 ENST00000243786.2 INHA AATTCAAAAATGGAGGTTACTCTTTCAAGTACTCGAGTACTTGAAAGAGTAACCTCCA 2722 chr2 ENST00000243786.2 INHBA AATTCAAAAAAGGCACTTTCCTACCCAATTACTCGAGTAATTGGGTAGGAAAGTGCCT 2723 chr7 ENST00000242208.4 INHBA AATTCAAAAAGAGAATGGTGTACCCTTTATTCTCGAGAATAAAGGGTACACCATTCTC 2724 chr7 ENST00000242208.4 INHBA AATTCAAAAAAGACGCTGCACTTCGAGATTTCTCGAGAAATCTCGAAGTGCAGCGTCT 2725 chr7 ENST00000242208.4 INHBB AATTCAAAAACAAATGGATGCGGTGACAAATCTCGAGATTTGTCACCGCATCCATTTG 2726 chr2 ENST00000295228.3 INHBB AATTCAAAAAGCTGGAACGACTGGATCATAGCTCGAGCTATGATCCAGTCGTTCCAGC 2727 chr2 ENST00000295228.3 INHBB AATTCAAAAATGATGAGTACAACATCGTCAACTCGAGTTGACGATGTTGTACTCATCA 2728 chr2 ENST00000295228.3 INHBC AATTCAAAAATCAACCAGACTCGTCTTGATTCTCGAGAATCAAGACGAGTCTGGTTGA 2729 chr12 ENST00000309668.2 INHBC AATTCAAAAACAAGACTGACATACCTGACATCTCGAGATGTCAGGTATGTCAGTCTTG 2730 chr12 ENST00000309668.2 INHBC AATTCAAAAACAGGCCAGTCTCATGTTCTTTCTCGAGAAAGAACATGAGACTGGCCTG 2731 chr12 ENST00000309668.2 INHBE AATTCAAAAACTCCTCTACCTGGATCATAATCTCGAGATTATGATCCAGGTAGAGGAG 2732 chr12 ENST00000266646.2 INHBE AATTCAAAAAACCTGGGCTGGCATACCTTAACTCGAGTTAAGGTATGCCAGCCCAGGT 2733 chr12 ENST00000266646.2 INHBE AATTCAAAAAGCAGCCCTTCCTAGAGCTTAACTCGAGTTAAGCTCTAGGAAGGGCTGC 2734 chr12 ENST00000266646.2 ITGA4 AATTCAAAAACCAACGCTTCAGTGATCAATCCTCGAGGATTGATCACTGAAGCGTTGG 2735 chr2 ENST00000397033.6 ITGA4 AATTCAAAAATGTAGAACACATCAAGCATTTCTCGAGAAATGCTTGATGTGTTCTACA 2736 chr2 ENST00000397033.6 ITGA4 AATTCAAAAACATGATCTTGTGACATATTATCTCGAGATAATATGTCACAAGATCATG 2737 chr2 ENST00000397033.6 ITGAV AATTCAAAAATTGAAGTGTACCCTAGCATTTCTCGAGAAATGCTAGGGTACACTTCAA 2738 chr2 ENST00000261023.7 ITGAV AATTCAAAAACACTCCAAGAACATGACTATTCTCGAGAATAGTCATGTTCTTGGAGTG 2739 chr2 ENST00000261023.7 ITGAV AATTCAAAAAGTGAGGTCGAAACAGGATAAACTCGAGTTTATCCTGTTTCGACCTCAC 2740 chr2 ENST00000261023.7 ITGB1 AATTCAAAAATTTGTAGGAAGAGGGATAATACTCGAGTATTATCCCTCTTCCTACAAA 2741 chr10 ENST00000302278.7 ITGB1 AATTCAAAAAGCCTTGCATTACTGCTGATATCTCGAGATATCAGCAGTAATGCAAGGC 2742 chr10 ENST00000302278.7 ITGB1 AATTCAAAAAGCCTTGCATTACTGCTGATATCTCGAGATATCAGCAGTAATGCAAGGC 2743 chr10 ENST00000302278.7 ITGB3 AATTCAAAAAGTCGTCAGATTCCAGTACTATCTCGAGATAGTACTGGAATCTGACGAC 2744 chr17 ENST00000559488.5 ITGB3 AATTCAAAAAGTCGTCAGATTCCAGTACTATCTCGAGATAGTACTGGAATCTGACGAC 2745 chr17 ENST00000559488.5 ITGB3 AATTCAAAAACCACGTCTACCTTCACCAATACTCGAGTATTGGTGAAGGTAGACGTGG 2746 chr17 ENST00000559488.5 KIT AATTCAAAAAACTTCATCTAACGAGATTAAACTCGAGTTTAATCTCGTTAGATGAAGT 2747 chr4 ENST00000288135.5 KIT AATTCAAAAAGCGACGAGATTAGGCTGTTATCTCGAGATAACAGCCTAATCTCGTCGC 2748 chr4 ENST00000288135.5 KIT AATTCAAAAAACGAGTTGGCCCTAGACTTAGCTCGAGCTAAGTCTAGGGCCAACTCGT 2749 chr4 ENST00000288135.5 KITLG AATTCAAAAAGCAGGAATCGTGTGACTAATACTCGAGTATTAGTCACACGATTCCTGC 2750 chr12 ENST00000228280.9 KITLG AATTCAAAAAGCAGGAATCGTGTGACTAATACTCGAGTATTAGTCACACGATTCCTGC 2751 chr12 ENST00000228280.9 KITLG AATTCAAAAACCTATTTAATCCTCTCGTCAACTCGAGTTGACGAGAGGATTAAATAGG 2752 chr12 ENST00000228280.9 KLHL20 AATTCAAAAAGCCAATACATGGAGGTTATATCTCGAGATATAACCTCCATGTATTGGC 2753 chr1 ENST00000209884.4 KLHL20 AATTCAAAAAGCCGCAAGAACGACCACTAATCTCGAGATTAGTGGTCGTTCTTGCGGC 2754 chr1 ENST00000209884.4 KLHL20 AATTCAAAAACACATTGTGAATCCCATATTTCTCGAGAAATATGGGATTCACAATGTG 2755 chr1 ENST00000209884.4 LEFTY1 AATTCAAAAAACAAGTTACCTCACCTAATTTCTCGAGAAATTAGGTGAGGTAACTTGT 2756 chr1 ENST00000272134.5 LEFTY1 AATTCAAAAAAGCCCAATGTGTCATTGTTTACTCGAGTAAACAATGACACATTGGGCT 2757 chr1 ENST00000272134.5 LEFTY1 AATTCAAAAATCTCTAGTGAGCCCTGAATTTCTCGAGAAATTCAGGGCTCACTAGAGA 2758 chr1 ENST00000272134.5 LEFTY2 AATTCAAAAAAGTTACTCCATCCCAATTTAGCTCGAGCTAAATTGGGATGGAGTAACT 2759 chr1 ENST00000366820.9 LEFTY2 AATTCAAAAACTAAGCACTTACGTGAGTAAACTCGAGTTTACTCACGTAAGTGCTTAG 2760 chr1 ENST00000366820.9 LEFTY2 AATTCAAAAATAGGCGCCTGGTGTATCCATTCTCGAGAATGGATACACCAGGCGCCTA 2761 chr1 ENST00000366820.9 LIF AATTCAAAAAGCAGTGCCAATGCCCTCTTTACTCGAGTAAAGAGGGCATTGGCACTGC 2762 chr22 ENST00000249075.3 LIF AATTCAAAAAACCGCATAGTCGTGTACCTTGCTCGAGCAAGGTACACGACTATGCGGT 2763 chr22 ENST00000249075.3 LIF AATTCAAAAACAACAACCTGGACAAGCTATGCTCGAGCATAGCTTGTCCAGGTTGTTG 2764 chr22 ENST00000249075.3 LIFR AATTCAAAAATGACTTGCGACTACGTCATTACTCGAGTAATGACGTAGTCGCAAGTCA 2765 chr5 ENST00000263409.8 LIFR AATTCAAAAAACTTCTGCAGATTCGATATTACTCGAGTAATATCGAATCTGCAGAAGT 2766 chr5 ENST00000263409.8 LIFR AATTCAAAAAGTAGGCTCAGACATAACATTTCTCGAGAAATGTTATGTCTGAGCCTAC 2767 chr5 ENST00000263409.8 LTA AATTCAAAAAGCCCTAGTACTGTCTTCTTTGCTCGAGCAAAGAAGACAGTACTAGGGC 2768 chr6 ENST00000418386.2 LTA AATTCAAAAAGATCAAGTCACCGGAGCTTTCCTCGAGGAAAGCTCCGGTGACTTGATC 2769 chr6 ENST00000418386.2 LTA AATTCAAAAAGCTCCCAGAAGATGGTGTATCCTCGAGGATACACCATCTTCTGGGAGC 2770 chr6 ENST00000418386.2 LTB AATTCAAAAAGCGAGAGGGAAGACCTTCTTTCTCGAGAAAGAAGGTCTTCCCTCTCGC 2771 chr6 ENST00000429299.2 LTB AATTCAAAAACGAGAGGGTGTACGTCAACATCTCGAGATGTTGACGTACACCCTCTCG 2772 chr6 ENST00000429299.2 LTB AATTCAAAAAGACGAAGGAACAGGCGTTTCTCTCGAGAGAAACGCCTGTTCCTTCGTC 2773 chr6 ENST00000429299.2 LTBP1 AATTCAAAAAGATGACCTGTGTCGATGTAAACTCGAGTTTACATCGACACAGGTCATC 2774 chr2 ENST00000407925.5 LTBP1 AATTCAAAAAGGTGGAACAGTGCTGTTATTTCTCGAGAAATAACAGCACTGTTCCACC 2775 chr2 ENST00000407925.5 LTBP1 AATTCAAAAACCGTTGAATACCGCCTTGAATCTCGAGATTCAAGGCGGTATTCAACGG 2776 chr2 ENST00000407925.5 LTBP3 AATTCAAAAAGCATCCTCAATGGATGTGAAACTCGAGTTTCACATCCATTGAGGATGC 2777 chr11 ENST00000322147.8 LTBP3 AATTCAAAAATGTTGTTCGGGTCGGAGATTTCTCGAGAAATCTCCGACCCGAACAACA 2778 chr11 ENST00000322147.8 LTBP3 AATTCAAAAAAGCGCTTCAAGGTGGTCTTTGCTCGAGCAAAGACCACCTTGAAGCGCT 2779 chr11 ENST00000322147.8 LTBP4 AATTCAAAAAGCTTCGACATGCCAGACTTTGCTCGAGCAAAGTCTGGCATGTCGAAGC 2780 chr19 ENST00000308370.11 LTBP4 AATTCAAAAATGAAACACTACAGGGTGTATGCTCGAGCATACACCCTGTAGTGTTTCA 2781 chr19 ENST00000308370.11 LTBP4 AATTCAAAAACAACCGGCTTTGAAAGAGTTACTCGAGTAACTCTTTCAAAGCCGGTTG 2782 chr19 ENST00000308370.11 MAF AATTCAAAAATCAGTGGGATACGCCACATTTCTCGAGAAATGTGGCGTATCCCACTGA 2783 chr16 ENST00000326043.4 MAF AATTCAAAAATTTATGGTGTGTGCAAGTAAACTCGAGTTTACTTGCACACACCATAAA 2784 chr16 ENST00000326043.4 MAF AATTCAAAAAGTTAGAGAAGAAGGCTATTAACTCGAGTTAATAGCCTTCTTCTCTAAC 2785 chr16 ENST00000326043.4 MAF AATTCAAAAATGTTAATGACTTCGATCTGATCTCGAGATCAGATCGAAGTCATTAACA 2786 chr16 ENST00000326043.4 MIF AATTCAAAAACTACATCAACTATTACGACATCTCGAGATGTCGTAATAGTTGATGTAG 2787 chr22 ENST00000215754.7 MIF AATTCAAAAACTACATCAACTATTACGACATCTCGAGATGTCGTAATAGTTGATGTAG 2788 chr22 ENST00000215754.7 MIF AATTCAAAAAGACAGGGTCTACATCAACTATCTCGAGATAGTTGATGTAGACCCTGTC 2789 chr22 ENST00000215754.7 MINOS1- AATTCAAAAAGCCAAGCTGCACAATTTAATACTCGAGTATTAAATTGTGCAGCTTGGC 2790 chr1 ENST00000602662.1 MINOS1- AATTCAAAAAGCTGGCACTGTTCCCAGATAACTCGAGTTATCTGGGAACAGTGCCAGC 2791 chr1 ENST00000602662.1 MINOS1- AATTCAAAAAAGAAAGACCACTGGCAGAAACCTCGAGGTTTCTGCCAGTGGTCTTTCT 2792 chr1 ENST00000602662.1 MSTN AATTCAAAAAAGGCCCAACTATGGATATATTCTCGAGAATATATCCATAGTTGGGCCT 2793 chr2 ENST00000260950.4 MSTN AATTCAAAAAGAGCTAGAAGGAGATCAAATTCTCGAGAATTTGATCTCCTTCTAGCTC 2794 chr2 ENST00000260950.4 MSTN AATTCAAAAAGTATGCTTTAAAGTCTATTTCCTCGAGGAAATAGACTTTAAAGCATAC 2795 chr2 ENST00000260950.4 NAMPT AATTCAAAAAAGCGATAGCTATGACATTTATCTCGAGATAAATGTCATAGCTATCGCT 2796 chr7 ENST00000222553.7 NAMPT AATTCAAAAAGTGAAGATCTAAGACATTTAACTCGAGTTAAATGTCTTAGATCTTCAC 2797 chr7 ENST00000222553.7 NAMPT AATTCAAAAATACAAGGTTACTCACTATAAACTCGAGTTTATAGTGAGTAACCTTGTA 2798 chr7 ENST00000222553.7 NBL1 AATTCAAAAAGCCAAGCTGCACAATTTAATACTCGAGTATTAAATTGTGCAGCTTGGC 2799 chr1 ENST00000375136.7 NBL1 AATTCAAAAAGCTGGCACTGTTCCCAGATAACTCGAGTTATCTGGGAACAGTGCCAGC 2800 chr1 ENST00000375136.7 NBL1 AATTCAAAAAAGAAAGACCACTGGCAGAAACCTCGAGGTTTCTGCCAGTGGTCTTTCT 2801 chr1 ENST00000375136.7 NDP AATTCAAAAACTGCTAAAGGTTACCGATTTCCTCGAGGAAATCGGTAACCTTTAGCAG 2802 chrX ENST00000378062.5 NDP AATTCAAAAACTCTGCATATTCTAGTAATAACTCGAGTTATTACTAGAATATGCAGAG 2803 chrX ENST00000378062.5 NDP AATTCAAAAAACGGACAGCTCATTCATAATGCTCGAGCATTATGAATGAGCTGTCCGT 2804 chrX ENST00000378062.5 NLRP7 AATTCAAAAACCGTTCAAGGAAATTTCTATTCTCGAGAATAGAAATTTCCTTGAACGG 2805 chr19 ENST00000328092.9 NLRP7 AATTCAAAAACGGGTCTCTAAGATGTCTTATCTCGAGATAAGACATCTTAGAGACCCG 2806 chr19 ENST00000328092.9 NLRP7 AATTCAAAAAACCTGCTCAGAAATCATAAATCTCGAGATTTATGATTTCTGAGCAGGT 2807 chr19 ENST00000328092.9 NODAL AATTCAAAAAGTGCTCCTAGATCACCATAAACTCGAGTTTATGGTGATCTAGGAGCAC 2808 chr10 ENST00000287139.7 NODAL AATTCAAAAACACCTATAGCTTTCATGTATTCTCGAGAATACATGAAAGCTATAGGTG 2809 chr10 ENST00000287139.7 NODAL AATTCAAAAAGCATGCTGTATGTGGATAATGCTCGAGCATTATCCACATACAGCATGC 2810 chr10 ENST00000287139.7 NOG AATTCAAAAAAGGTCAGTATTATACGTTAAACTCGAGTTTAACGTATAATACTGACCT 2811 chr17 ENST00000332822.4 NOG AATTCAAAAAATTCTGGTTGTTGCTAATAATCTCGAGATTATTAGCAACAACCAGAAT 2812 chr17 ENST00000332822.4 NOG AATTCAAAAATGCGGAGGAAGTTACAGATGTCTCGAGACATCTGTAACTTCCTCCGCA 2813 chr17 ENST00000332822.4 NRG1 AATTCAAAAAGATATCACAGAGGCCTATAACCTCGAGGTTATAGGCCTCTGTGATATC 2814 chr8 ENST00000287842.7 NRG1 AATTCAAAAAGGCTGATTCTGGAGAGTATATCTCGAGATATACTCTCCAGAATCAGCC 2815 chr8 ENST00000287842.7 NRG1 AATTCAAAAAGACAGTGCCTCTGCCAATATCCTCGAGGATATTGGCAGAGGCACTGTC 2816 chr8 ENST00000287842.7 NRP1 AATTCAAAAATATACTAGAATCACCGCATTTCTCGAGAAATGCGGTGATTCTAGTATA 2817 chr10 ENST00000265371.8 NRP1 AATTCAAAAACAGCCTTGAATGCACTTATATCTCGAGATATAAGTGCATTCAAGGCTG 2818 chr10 ENST00000265371.8 NRP1 AATTCAAAAACAGCCTTGAATGCACTTATATCTCGAGATATAAGTGCATTCAAGGCTG 2819 chr10 ENST00000265371.8 NRP2 AATTCAAAAACGACTGCAAGTATGACTTTATCTCGAGATAAAGTCATACTTGCAGTCG 2820 chr2 ENST00000357785.9 NRP2 AATTCAAAAACCGGATTGCTAATGAACAGATCTCGAGATCTGTTCATTAGCAATCCGG 2821 chr2 ENST00000357785.9 NRP2 AATTCAAAAACCTCAACTTCAACCCTCACTTCTCGAGAAGTGAGGGTTGAAGTTGAGG 2822 chr2 ENST00000357785.9 OSM AATTCAAAAAACTTCCTCCTTTCCGTGTTTCCTCGAGGAAACACGGAAAGGAGGAAGT 2823 chr22 ENST00000215781.2 OSM AATTCAAAAAGGACCGACTTTCCATTGATTCCTCGAGGAATCAATGGAAAGTCGGTCC 2824 chr22 ENST00000215781.2 OSM AATTCAAAAATGGTCCTTGCACTCCTGTTTCCTCGAGGAAACAGGAGTGCAAGGACCA 2825 chr22 ENST00000215781.2 OSMR AATTCAAAAATAACCTGACTCATCGAGTTTACTCGAGTAAACTCGATGAGTCAGGTTA 2826 chr5 ENST00000274276.7 OSMR AATTCAAAAAAGGAGAACCCTCACCTAATAACTCGAGTTATTAGGTGAGGGTTCTCCT 2827 chr5 ENST00000274276.7 OSMR AATTCAAAAAGCACTCCATAAGGAATAATTTCTCGAGAAATTATTCCTTATGGAGTGC 2828 chr5 ENST00000274276.7 PARK7 AATTCAAAAAGTAGCCGTGATGTGGTCATTTCTCGAGAAATGACCACATCACGGCTAC 2829 chr1 ENST00000338639.9 PARK7 AATTCAAAAAGCAATTGTTGAAGCCCTGAATCTCGAGATTCAGGGCTTCAACAATTGC 2830 chr1 ENST00000338639.9 PARK7 AATTCAAAAAACTCTGAGAATCGTGTGGAAACTCGAGTTTCCACACGATTCTCAGAGT 2831 chr1 ENST00000338639.9 PDPN AATTCAAAAAGCCTCTGGTATGAGAAATAAACTCGAGTTTATTTCTCATACCAGAGGC 2832 chr1 ENST00000294489.10 PDPN AATTCAAAAAAGTCCACGCGCAAGAACAAAGCTCGAGCTTTGTTCTTGCGCGTGGACT 2833 chr1 ENST00000294489.10 PDPN AATTCAAAAATGACCCTGGTTGGAATCATAGCTCGAGCTATGATTCCAACCAGGGTCA 2834 chr1 ENST00000294489.10 PF4 AATTCAAAAAACGCTGAAGAATGGAAGGAAACTCGAGTTTCCTTCCATTCTTCAGCGT 2835 chr4 ENST00000296029.3 PF4 AATTCAAAAACCAACTGATAGCCACGCTGAACTCGAGTTCAGCGTGGCTATCAGTTGG 2836 chr4 ENST00000296029.3 PF4 AATTCAAAAACACGCTGAAGAATGGAAGGAACTCGAGTTCCTTCCATTCTTCAGCGTG 2837 chr4 ENST00000296029.3 PF4V1 AATTCAAAAAGTTGTGGTATAGTCAATCTATCTCGAGATAGATTGACTATACCACAAC 2838 chr4 ENST00000226524.3 PF4V1 AATTCAAAAAAGCTGCCTAAGTGTGCACTTTCTCGAGAAAGTGCACACTTAGGCAGCT 2839 chr4 ENST00000226524.3 PF4V1 AATTCAAAAACTGACACATCACAATTTCATACTCGAGTATGAAATTGTGATGTGTCAG 2840 chr4 ENST00000226524.3 PGLYRP1 AATTCAAAAAGTGCCCACTCAGGTCACTTATCTCGAGATAAGTGACCTGAGTGGGCAC 2841 chr19 ENST00000008938.4 PGLYRP1 AATTCAAAAACTTACGCTATGTGGTGGTATCCTCGAGGATACCACCACATAGCGTAAG 2842 chr19 ENST00000008938.4 PGLYRP1 AATTCAAAAACATCAGCTTCATGGGCAACTACTCGAGTAGTTGCCCATGAAGCTGATG 2843 chr19 ENST00000008938.4 PLP2 AATTCAAAAACCTGTCGGTGATTGAGATGATCTCGAGATCATCTCAATCACCGACAGG 2844 chrX ENST00000376327.5 PLP2 AATTCAAAAACCTGTCGGTGATTGAGATGATCTCGAGATCATCTCAATCACCGACAGG 2845 chrX ENST00000376327.5 PLP2 AATTCAAAAACGAAAGGGAATCCTCCTGTTTCTCGAGAAACAGGAGGATTCCCTTTCG 2846 chrX ENST00000376327.5 PPBP AATTCAAAAAAGGTGATGAATCTGCTGATTACTCGAGTAATCAGCAGATTCATCACCT 2847 chr4 ENST00000296028.3 PPBP AATTCAAAAATGTTTCTGCCAAACTTCTTTACTCGAGTAAAGAAGTTTGGCAGAAACA 2848 chr4 ENST00000296028.3 PPBP AATTCAAAAACTCCCAGGAAGGGTAGAATTTCTCGAGAAATTCTACCCTTCCTGGGAG 2849 chr4 ENST00000296028.3 PXDN AATTCAAAAAAGATTGCGACTGGACTCAAACCTCGAGGTTTGAGTCCAGTCGCAATCT 2850 chr2 ENST00000252804.8 PXDN AATTCAAAAAGTTCCTGACGTCAGTCGAAATCTCGAGATTTCGACTGACGTCAGGAAC 2851 chr2 ENST00000252804.8 PXDN AATTCAAAAAGAAGGATTCTTGACCATCAATCTCGAGATTGATGGTCAAGAATCCTTC 2852 chr2 ENST00000252804.8 RORC AATTCAAAAACACCTCACAAATTGAAGTGATCTCGAGATCACTTCAATTTGTGAGGTG 2853 chr1 ENST00000318247.6 RORC AATTCAAAAAGCCCTCATATTCCAACAACTTCTCGAGAAGTTGTTGGAATATGAGGGC 2854 chr1 ENST00000318247.6 RORC AATTCAAAAAGCTTCTCAAAGCAGGAGCAATCTCGAGATTGCTCCTGCTTTGAGAAGC 2855 chr1 ENST00000318247.6 RORC AATTCAAAAACGAGGATGAGATTGCCCTCTACTCGAGTAGAGGGCAATCTCATCCTCG 2856 chr1 ENST00000318247.6 SCG2 AATTCAAAAAACGACAAGGATCAAGAATTAGCTCGAGCTAATTCTTGATCCTTGTCGT 2857 chr2 ENST00000305409.2 SCG2 AATTCAAAAACCTGTCTCTTATCCCTTTAATCTCGAGATTAAAGGGATAAGAGACAGG 2858 chr2 ENST00000305409.2 SCG2 AATTCAAAAAGAAAGCAGCCCAGATTATAATCTCGAGATTATAATCTGGGCTGCTTTC 2859 chr2 ENST00000305409.2 SCGB3A1 AATTCAAAAATCATAGAGGGCTCCCAGAAGTCTCGAGACTTCTGGGAGCCCTCTATGA 2860 chr5 ENST00000292641.3 SCGB3A1 AATTCAAAAACCCGTGAACCACCTCATAGAGCTCGAGCTCTATGAGGTGGTTCACGGG 2861 chr5 ENST00000292641.3 SCGB3A1 AATTCAAAAAGACTGGAGCATCTACACCTGACTCGAGTCAGGTGTAGATGCTCCAGTC 2862 chr5 ENST00000292641.3 SECTM1 AATTCAAAAACACCAGAGAAATAACAGACAACTCGAGTTGTCTGTTATTTCTCTGGTG 2863 chr17 ENST00000269389.7 SECTM1 AATTCAAAAACCATGACTCGAATATCTGAAACTCGAGTTTCAGATATTCGAGTCATGG 2864 chr17 ENST00000269389.7 SECTM1 AATTCAAAAACCATGACTCGAATATCTGAAACTCGAGTTTCAGATATTCGAGTCATGG 2865 chr17 ENST00000269389.7 SLURP1 AATTCAAAAAGTGCTTCCTGCAGGACCATTACTCGAGTAATGGTCCTGCAGGAAGCAC 2866 chr8 ENST00000246515.1 SLURP1 AATTCAAAAAAGACCTCTGCAACTCGGAACTCTCGAGAGTTCCGAGTTGCAGAGGTCT 2867 chr8 ENST00000246515.1 SLURP1 AATTCAAAAACTCAAGTGCTACACCTGCAAGCTCGAGCTTGCAGGTGTAGCACTTGAG 2868 chr8 ENST00000246515.1 SOSTDC1 AATTCAAAAAGATGCCACAGAAATCCTTTATCTCGAGATAAAGGATTTCTGTGGCATC 2869 chr7 ENST00000307068.4 SOSTDC1 AATTCAAAAAGGAACTGCGTTCCACCAAATACTCGAGTATTTGGTGGAACGCAGTTCC 2870 chr7 ENST00000307068.4 SOSTDC1 AATTCAAAAATGAATCTTCACAGTAACATTTCTCGAGAAATGTTACTGTGAAGATTCA 2871 chr7 ENST00000307068.4 SP100 AATTCAAAAAGAAGTGAGCCTGTGATCAATACTCGAGTATTGATCACAGGCTCACTTC 2872 chr2 ENST00000340126.8 SP100 AATTCAAAAATATACGCTGCGGTGGATATACCTCGAGGTATATCCACCGCAGCGTATA 2873 chr2 ENST00000340126.8 SP100 AATTCAAAAATCGTGATCTCATCACAAATAACTCGAGTTATTTGTGATGAGATCACGA 2874 chr2 ENST00000340126.8 SPI1 AATTCAAAAAGCCCTATGACACGGATCTATACTCGAGTATAGATCCGTGTCATAGGGC 2875 chr11 ENST00000378538.7 SPI1 AATTCAAAAAAGAGCTTCGCCGAGAACAACTCTCGAGAGTTGTTCTCGGCGAAGCTCT 2876 chr11 ENST00000378538.7 SPI1 AATTCAAAAACGGATCTATACCAACGCCAAACTCGAGTTTGGCGTTGGTATAGATCCG 2877 chr11 ENST00000378538.7 SPI1 AATTCAAAAACCGTATGTAAATCAGATCTCCCTCGAGGGAGATCTGATTTACATACGG 2878 chr11 ENST00000378538.7 SPP1 AATTCAAAAACCACAAGCAGTCCAGATTATACTCGAGTATAATCTGGACTGCTTGTGG 2879 chr4 ENST00000237623.11 SPP1 AATTCAAAAACCGAGGTGATAGTGTGGTTTACTCGAGTAAACCACACTATCACCTCGG 2880 chr4 ENST00000237623.11 SPP1 AATTCAAAAACTTCAGGGTTATGTCTATGTTCTCGAGAACATAGACATAACCCTGAAG 2881 chr4 ENST00000237623.11 TBX21 AATTCAAAAAGCCCTAACTACAGTCGTTTACCTCGAGGTAAACGACTGTAGTTAGGGC 2882 ch17 ENST00000177694.1 TBX21 AATTCAAAAACCTGTTGTGGTCCAAGTTTAACTCGAGTTAAACTTGGACCACAACAGG 2883 ch17 ENST00000177694.1 TBX21 AATTCAAAAACGCTTCCAACACGCATATCTTCTCGAGAAGATATGCGTGTTGGAAGCG 2884 ch17 ENST00000177694.1 TBX21 AATTCAAAAAACAATGTGACCCAGATGATTGCTCGAGCAATCATCTGGGTCACATTGT 2885 ch17 ENST00000177694.1 TCAP AATTCAAAAACTTTGTAGTTTGCCCAGAGTTCTCGAGAACTCTGGGCAAACTACAAAG 2886 chr17 ENST00000309889.2 TCAP AATTCAAAAAGGCCATGGCTGCTTTGTAGTTCTCGAGAACTACAAAGCAGCCATGGCC 2887 chr17 ENST00000309889.2 TCAP AATTCAAAAAGGTGGCTGAGATCACAAAGCACTCGAGTGCTTTGTGATCTCAGCCACC 2888 chr17 ENST00000309889.2 TGFB1 AATTCAAAAAACTGCGGATCTCTGTGTCATTCTCGAGAATGACACAGAGATCCGCAGT 2889 chr19 ENST00000221930.5 TGFB1 AATTCAAAAACCACAACGAAATCTATGACAACTCGAGTTGTCATAGATTTCGTTGTGG 2890 chr19 ENST00000221930.5 TGFB1 AATTCAAAAACCACAACGAAATCTATGACAACTCGAGTTGTCATAGATTTCGTTGTGG 2891 chr19 ENST00000221930.5 TGFB2 AATTCAAAAAGCGGCCTATTGCTTTAGAAATCTCGAGATTTCTAAAGCAATAGGCCGC 2892 chr1 ENST00000366930.8 TGFB2 AATTCAAAAAGCTGGAGCATGCCCGTATTTACTCGAGTAAATACGGGCATGCTCCAGC 2893 chr1 ENST00000366930.8 TGFB2 AATTCAAAAATTGCTGCCTACGTCCACTTTACTCGAGTAAAGTGGACGTAGGCAGCAA 2894 chr1 ENST00000366930.8 TGFB3 AATTCAAAAACATTGCCAAACAGCGCTATATCTCGAGATATAGCGCTGTTTGGCAATG 2895 chr14 ENST00000238682.7 TGFB3 AATTCAAAAAGCTCTAGGGAATCTGGATTATCTCGAGATAATCCAGATTCCCTAGAGC 2896 chr14 ENST00000238682.7 TGFB3 AATTCAAAAACGGAATACTATGCCAAAGAAACTCGAGTTTCTTTGGCATAGTATTCCG 2897 chr14 ENST00000238682.7 TGFBR1 AATTCAAAAAGCCTTGAGAGTAATGGCTAAACTCGAGTTTAGCCATTACTCTCAAGGC 2898 chr9 ENST00000374994.8 TGFBR1 AATTCAAAAACTCATGTTGATGGTCTATATCCTCGAGGATATAGACCATCAACATGAG 2899 chr9 ENST00000374994.8 TGFBR1 AATTCAAAAAGAAGTTGCTGTTAAGATATTCCTCGAGGAATATCTTAACAGCAACTTC 2900 chr9 ENST00000374994.8 TGFBR2 AATTCAAAAACGTTCAGAAGTCGGTTAATAACTCGAGTTATTAACCGACTTCTGAACG 2901 chr3 ENST00000295754.9 TGFBR2 AATTCAAAAACTCTAGGCTTTATCGTGTTTACTCGAGTAAACACGATAAAGCCTAGAG 2902 chr3 ENST00000295754.9 TGFBR2 AATTCAAAAACTCAGGAAATGAGATTGATTTCTCGAGAAATCAATCTCATTTCCTGAG 2903 chr3 ENST00000295754.9 TGFBR3 AATTCAAAAAGGAGTTGGTAAAGGGTTAATACTCGAGTATTAACCCTTTACCAACTCC 2904 chr1 ENST00000212355.8 TGFBR3 AATTCAAAAATAATGGATTTCCGGGAGATATCTCGAGATATCTCCCGGAAATCCATTA 2905 chr1 ENST00000212355.8 TGFBR3 AATTCAAAAACACACCCAGGGCTAGTATAAACTCGAGTTTATACTAGCCCTGGGTGTG 2906 chr1 ENST00000212355.8 THBS1 AATTCAAAAAGTAGGTTATGATGAGTTTAATCTCGAGATTAAACTCATCATAACCTAC 2907 chr15 ENST00000260356.5 THBS1 AATTCAAAAACGTGACTGTAAGATTGTAAATCTCGAGATTTACAATCTTACAGTCACG 2908 chr15 ENST00000260356.5 THBS1 AATTCAAAAAGAGATCCCTAATCATCAAATTCTCGAGAATTTGATGATTAGGGATCTC 2909 chr15 ENST00000260356.5 THNSL2 AATTCAAAAAGAGCCGATCAAGACTGTGTTTCTCGAGAAACACAGTCTTGATCGGCTC 2910 chr2 ENST00000324166.6 THNSL2 AATTCAAAAAGCTGCCATTGAGAGTGTTCAACTCGAGTTGAACACTCTCAATGGCAGC 2911 chr2 ENST00000324166.6 THNSL2 AATTCAAAAAGCTGCCATTGAGAGTGTTCAACTCGAGTTGAACACTCTCAATGGCAGC 2912 chr2 ENST00000324166.6 THPO AATTCAAAAAGACCTCCGAGTCCTCAGTAAACTCGAGTTTACTGAGGACTCGGAGGTC 2913 chr3 ENST00000204615.11 THPO AATTCAAAAAAGCTAGCTCTTTGGTCTATTTCTCGAGAAATAGACCAAAGAGCTAGCT 2914 chr3 ENST00000204615.11 THPO AATTCAAAAACAACCTCCAGCCTGGATATTCCTCGAGGAATATCCAGGCTGGAGGTTG 2915 chr3 ENST00000204615.11 TIMP1 AATTCAAAAAGCACAGTGTTTCCCTGTTTATCTCGAGATAAACAGGGAAACACTGTGC 2916 chrX ENST00000218388.8 TIMP1 AATTCAAAAAGCACAGTGTTTCCCTGTTTATCTCGAGATAAACAGGGAAACACTGTGC 2917 chrX ENST00000218388.8 TIMP1 AATTCAAAAAACAGACGGCCTTCTGCAATTCCTCGAGGAATTGCAGAAGGCCGTCTGT 2918 chrX ENST00000218388.8 TNF AATTCAAAAAGAACCCAAGCTTAGAACTTTACTCGAGTAAAGTTCTAAGCTTGGGTTC 2919 chr6 ENST00000449264.2 TNF AATTCAAAAAGGAGCCAGCTCCCTCTATTTACTCGAGTAAATAGAGGGAGCTGGCTCC 2920 chr6 ENST00000449264.2 TNF AATTCAAAAATGGCGTGGAGCTGAGAGATAACTCGAGTTATCTCTCAGCTCCACGCCA 2921 chr6 ENST00000449264.2 TNFRSF4 AATTCAAAAAGCACGTGGTGTAACCTCAGAACTCGAGTTCTGAGGTTACACCACGTGC 2922 chr1 ENST00000379236.3 TNFRSF4 AATTCAAAAACAGCAATAGCTCGGACGCAATCTCGAGATTGCGTCCGAGCTATTGCTG 2923 chr1 ENST00000379236.3 TNFRSF4 AATTCAAAAAGACAGCTACAAGCCTGGAGTTCTCGAGAACTCCAGGCTTGTAGCTGTC 2924 chr1 ENST00000379236.3 TNFRSF4 AATTCAAAAAGCTTCTACAACGACGTGGTCACTCGAGTGACCACGTCGTTGTAGAAGC 2925 chr1 ENST00000379236.3 TNFRSF11 AATTCAAAAATGTTTACTTGCCCGGTTTAATCTCGAGATTAAACCGGGCAAGTAAACA 2926 chr18 ENST00000586569.2 TNFRSF11 AATTCAAAAATGTACCAGTGAGAAGCATTATCTCGAGATAATGCTTCTCACTGGTACA 2927 chr18 ENST00000586569.2 TNFRSF11 AATTCAAAAATGGGACGGTGCTGTAACAAATCTCGAGATTTGTTACAGCACCGTCCCA 2928 chr18 ENST00000586569.2 TNFRSF11 AATTCAAAAAGAAAGCACTCACAGCTAATTTCTCGAGAAATTAGCTGTGAGTGCTTTC 2929 chr8 ENST00000297350.8 TNFRSF11 AATTCAAAAAGATAAATGCTTGCTGCATAAACTCGAGTTTATGCAGCAAGCATTTATC 2930 chr8 ENST00000297350.8 TNFRSF11 AATTCAAAAACCAGTGTGTGTTCATTGTAAACTCGAGTTTACAATGAACACACACTGG 2931 chr8 ENST00000297350.8 TNFRSF1A AATTCAAAAAAGAACCAGTACCGGCATTATTCTCGAGAATAATGCCGGTACTGGTTCT 2932 chr12 ENST00000162749.6 TNFRSF1A AATTCAAAAAGGAGCTGTTGGTGGGAATATACTCGAGTATATTCCCACCAACAGCTCC 2933 chr12 ENST00000162749.6 TNFRSF1A AATTCAAAAACTTGAAGGAACTACTACTAAGCTCGAGCTTAGTAGTAGTTCCTTCAAG 2934 chr12 ENST00000162749.6 TNFRSF9 AATTCAAAAAGCTCCGTTTCTCTGTTGTTAACTCGAGTTAACAACAGAGAAACGGAGC 2935 chr1 ENST00000377507.7 TNFRSF9 AATTCAAAAACAAGAACACCATCCTACATAACTCGAGTTATGTAGGATGGTGTTCTTG 2936 chr1 ENST00000377507.7 TNFRSF9 AATTCAAAAACAGTCCCTGTCCTCCAAATAGCTCGAGCTATTTGGAGGACAGGGACTG 2937 chr1 ENST00000377507.7 TNFSF9 AATTCAAAAACAAGTTGGACCTTGATATTTACTCGAGTAAATATCAAGGTCCAACTTG 2938 chr19 ENST00000245817.4 TNFSF9 AATTCAAAAACTACTATGTCTTCTTTCAACTCTCGAGAGTTGAAAGAAGACATAGTAG 2939 chr19 ENST00000245817.4 TNFSF9 AATTCAAAAACCCTTCACCGAGGTCGGAATACTCGAGTATTCCGACCTCGGTGAAGGG 2940 chr19 ENST00000245817.4 TNFSF9 AATTCAAAAATGAGCTACAAAGAGGACACGACTCGAGTCGTGTCCTCTTTGTAGCTCA 2941 chr19 ENST00000245817.4 TNFSF10 AATTCAAAAAAGAAATAGTTGTTGGTCTAAACTCGAGTTTAGACCAACAACTATTTCT 2942 chr3 ENST00000241261.6 TNFSF10 AATTCAAAAAAGTTATCCTGACCCTATATTGCTCGAGCAATATAGGGTCAGGATAACT 2943 chr3 ENST00000241261.6 TNFSF10 AATTCAAAAAGACAAACAAATGGTCCAATATCTCGAGATATTGGACCATTTGTTTGTC 2944 chr3 ENST00000241261.6 TNFSF11 AATTCAAAAACTAATGGTGTACGTCACTAAACTCGAGTTTAGTGACGTACACCATTAG 2945 chr13 ENST00000398795.6 TNFSF11 AATTCAAAAACCGGATCAGGATGCAACATACCTCGAGGTATGTTGCATCCTGATCCGG 2946 chr13 ENST00000398795.6 TNFSF11 AATTCAAAAAGCAGTATATTTCTTCGTTCTTCTCGAGAAGAACGAAGAAATATACTGC 2947 chr13 ENST00000398795.6 TNFSF12 AATTCAAAAAGTATTCCCACTCTTATCTTACCTCGAGGTAAGATAAGAGTGGGAATAC 2948 chr17 ENST00000293825.10 TNFSF12 AATTCAAAAAGGGCATTGTGTTCACTGTACTCTCGAGAGTACAGTGAACACAATGCCC 2949 chr17 ENST00000293825.10 TNFSF12 AATTCAAAAACAGATGGAGGTTACACAACTTCTCGAGAAGTTGTGTAACCTCCATCTG 2950 chr17 ENST00000293825.10 TNFSF12- AATTCAAAAACCTCACCTACTTCGGACTCTTCTCGAGAAGAGTCCGAAGTAGGTGAGG 2951 chr17 ENST00000293826.4 TNFSF12- AATTCAAAAACTGTACTGTCAGGTGCACTTTCTCGAGAAAGTGCACCTGACAGTACAG 2952 chr17 ENST00000293826.4 TNFSF12- AATTCAAAAAGCGCAGGCAGATGGAGGTTACCTCGAGGTAACCTCCATCTGCCTGCGC 2953 chr17 ENST00000293826.4 TNFSF13 AATTCAAAAACAGTTGCCCTCTGGTTGAGTTCTCGAGAACTCAACCAGAGGGCAACTG 2954 chr17 ENST00000338784.8 TNFSF13 AATTCAAAAAATGGCTCTGCTGACCCAACAACTCGAGTTGTTGGGTCAGCAGAGCCAT 2955 chr17 ENST00000338784.8 TNFSF13 AATTCAAAAACCCAACAAACAGAGCTGCAGACTCGAGTCTGCAGCTCTGTTTGTTGGG 2956 chr17 ENST00000338784.8 TNFSF13B AATTCAAAAACCTGAAACACTACCCAATAATCTCGAGATTATTGGGTAGTGTTTCAGG 2957 chr13 ENST00000375887.8 TNFSF13B AATTCAAAAACTACGCCATGGGACATCTAATCTCGAGATTAGATGTCCCATGGCGTAG 2958 chr13 ENST00000375887.8 TNFSF13B AATTCAAAAAGTGACTTTGTTTCGATGTATTCTCGAGAATACATCGAAACAAAGTCAC 2959 chr13 ENST00000375887.8 TNFSF14 AATTCAAAAATCCTGGGAGCAGCTGATACAACTCGAGTTGTATCAGCTGCTCCCAGGA 2960 chr19 ENST00000599359.1 TNFSF14 AATTCAAAAAGACAGACCGACATCCCATTCACTCGAGTGAATGGGATGTCGGTCTGTC 2961 chr19 ENST00000599359.1 TNFSF14 AATTCAAAAAATGGGTCTGACACGTGGAGAACTCGAGTTCTCCACGTGTCAGACCCAT 2962 chr19 ENST00000599359.1 TNFSF15 AATTCAAAAAATTAAGACACTGATCACTAAACTCGAGTTTAGTGATCAGTGTCTTAAT 2963 chr9 ENST00000374045.4 TNFSF15 AATTCAAAAAGTCGGGAGACTACTTCATTTACTCGAGTAAATGAAGTAGTCTCCCGAC 2964 chr9 ENST00000374045.4 TNFSF15 AATTCAAAAAACTATAGGAGGAGAGCAAATACTCGAGTATTTGCTCTCCTCCTATAGT 2965 chr9 ENST00000374045.4 TNFSF18 AATTCAAAAACCTTCAGTTGGCTAATCTTTACTCGAGTAAAGATTAGCCAACTGAAGG 2966 chr1 ENST00000404377.3 TNFSF18 AATTCAAAAACTGAACCTCCTTGCGTGAATACTCGAGTATTCACGCAAGGAGGTTCAG 2967 chr1 ENST00000404377.3 TNFSF18 AATTCAAAAAATGATACAAACTCTAACAAACCTCGAGGTTTGTTAGAGTTTGTATCAT 2968 chr1 ENST00000404377.3 TNFSF4 AATTCAAAAAGTGGCCTCTCTGACTTACAAACTCGAGTTTGTAAGTCAGAGAGGCCAC 2969 chr1 ENST00000281834.3 TNFSF4 AATTCAAAAAGCAGAACAACTCAGTCATCATCTCGAGATGATGACTGAGTTGTTCTGC 2970 chr1 ENST00000281834.3 TNFSF4 AATTCAAAAAGCCAAGATTCGAGAGGAACAACTCGAGTTGTTCCTCTCGAATCTTGGC 2971 chr1 ENST00000281834.3 TNFSF8 AATTCAAAAAACTGTATGGTCTTGATCTATTCTCGAGAATAGATCAAGACCATACAGT 2972 chr9 ENST00000223795.2 TNFSF8 AATTCAAAAACAAACTACACAGGGTATTAAACTCGAGTTTAATACCCTGTGTAGTTTG 2973 chr9 ENST00000223795.2 TNFSF8 AATTCAAAAAGTGGATACATTCCAGTACATACTCGAGTATGTACTGGAATGTATCCAC 2974 chr9 ENST00000223795.2 TNFSF9 AATTCAAAAACAAGTTGGACCTTGATATTTACTCGAGTAAATATCAAGGTCCAACTTG 2975 chr19 ENST00000245817.4 TNFSF9 AATTCAAAAACTACTATGTCTTCTTTCAACTCTCGAGAGTTGAAAGAAGACATAGTAG 2976 chr19 ENST00000245817.4 TNFSF9 AATTCAAAAACCCTTCACCGAGGTCGGAATACTCGAGTATTCCGACCTCGGTGAAGGG 2977 chr19 ENST00000245817.4 TRIM16 AATTCAAAAAGCCGTTGTTCAGCGCAAATATCTCGAGATATTTGCGCTGAACAACGGC 2978 chr17 ENST00000336708.11 TRIM16 AATTCAAAAAGCCGTTGTTCAGCGCAAATATCTCGAGATATTTGCGCTGAACAACGGC 2979 chr17 ENST00000336708.11 TRIM16 AATTCAAAAACCGCATCAGGTGAACATCAAACTCGAGTTTGATGTTCACCTGATGCGG 2980 chr17 ENST00000336708.11 TSLP AATTCAAAAAACTCAATGATAGCACCTAAACCTCGAGGTTTAGGTGCTATCATTGAGT 2981 chr5 ENST00000344895.3 TSLP AATTCAAAAACGTCGCTTCAATCGACCTTTACTCGAGTAAAGGTCGATTGAAGCGACG 2982 chr5 ENST00000344895.3 TSLP AATTCAAAAACCATCTTTATTATGGTCATATCTCGAGATATGACCATAATAAAGATGG 2983 chr5 ENST00000344895.3 TWSG1 AATTCAAAAAGACTGTGTTGGTATGTGTAATCTCGAGATTACACATACCAACACAGTC 2984 chr18 ENST00000262120.9 TWSG1 AATTCAAAAAGCGCCTTATTCCAGTGACAAACTCGAGTTTGTCACTGGAATAAGGCGC 2985 chr18 ENST00000262120.9 TWSG1 AATTCAAAAAGAATCACTGAGCTGTAACAAACTCGAGTTTGTTACAGCTCAGTGATTC 2986 chr18 ENST00000262120.9 TXLNA AATTCAAAAAGCACATACTGTGTGGACAATACTCGAGTATTGTCCACACAGTATGTGC 2987 chr1 ENST00000373609.1 TXLNA AATTCAAAAATGCTGATGCAGACATTGAATACTCGAGTATTCAATGTCTGCATCAGCA 2988 chr1 ENST00000373609.1 TXLNA AATTCAAAAAAGCGAGGTATTCACCACATTCCTCGAGGAATGTGGTGAATACCTCGCT 2989 chr1 ENST00000373609.1 VASN AATTCAAAAAAGCTTGACTACGCCGACTTTGCTCGAGCAAAGTCGGCGTAGTCAAGCT 2990 chr16 ENST00000304735.3 VASN AATTCAAAAAAGCCAACAGGCTGCATGAAATCTCGAGATTTCATGCAGCCTGTTGGCT 2991 chr16 ENST00000304735.3 VASN AATTCAAAAAGAGATCCTTTCCCATTTATTCCTCGAGGAATAAATGGGAAAGGATCTC 2992 chr16 ENST00000304735.3 VEGFA AATTCAAAAACAAGATCCGCAGACGTGTAAACTCGAGTTTACACGTCTGCGGATCTTG 2993 chr6 ENST00000425836.6 VEGFA AATTCAAAAACAAGATCCGCAGACGTGTAAACTCGAGTTTACACGTCTGCGGATCTTG 2994 chr6 ENST00000425836.6 VEGFA AATTCAAAAAGCGCAAGAAATCCCGGTATAACTCGAGTTATACCGGGATTTCTTGCGC 2995 chr6 ENST00000425836.6 VSTM1 AATTCAAAAAATGAATATGCGGCACTGAAAGCTCGAGCTTTCAGTGCCGCATATTCAT 2996 chr19 ENST00000338372.6 VSTM1 AATTCAAAAACATTCCCAGAATGTGACATTTCTCGAGAAATGTCACATTCTGGGAATG 2997 chr19 ENST00000338372.6 VSTM1 AATTCAAAAAGAGTGACCTATGCTGAGCTAACTCGAGTTAGCTCAGCATAGGTCACTC 2998 chr19 ENST00000338372.6 WFIKKN1 AATTCAAAAATGCGCCCTGATCAGATGTATGCTCGAGCATACATCTGATCAGGGCGCA 2999 chr16 ENST00000319070.2 WFIKKN1 AATTCAAAAAGGACGTGCTCAAGGATGACAACTCGAGTTGTCATCCTTGAGCACGTCC 3000 chr16 ENST00000319070.2 WFIKKN1 AATTCAAAAAAGTGCTGCATCAACGTGTGTGCTCGAGCACACACGTTGATGCAGCACT 3001 chr16 ENST00000319070.2 WFIKKN2 AATTCAAAAATCAAGTTCTTGGGCACCAAGTCTCGAGACTTGGTGCCCAAGAACTTGA 3002 chr17 ENST00000311378.4 WFIKKN2 AATTCAAAAATACAACCGCTGCTATATGGACCTCGAGGTCCATATAGCAGCGGTTGTA 3003 chr17 ENST00000311378.4 WFIKKN2 AATTCAAAAACACCAGCTTGCTCAGATATTCCTCGAGGAATATCTGAGCAAGCTGGTG 3004 chr17 ENST00000311378.4 WNT1 AATTCAAAAACTGTCGAGAAACGGCGTTTATCTCGAGATAAACGCCGTTTCTCGACAG 3005 chr12 ENST00000293549.3 WNT1 AATTCAAAAAGACCTCGTCTACTTCGAGAAACTCGAGTTTCTCGAAGTAGACGAGGTC 3006 chr12 ENST00000293549.3 WNT1 AATTCAAAAAGCCACGAGTTTGGATGTTGTACTCGAGTACAACATCCAAACTCGTGGC 3007 chr12 ENST00000293549.3 WNT2 AATTCAAAAACCACAAATGGTCCCAATTAAGCTCGAGCTTAATTGGGACCATTTGTGG 3008 chr7 ENST00000265441.7 WNT2 AATTCAAAAATCGGGAATCTGCCTTTGTTTACTCGAGTAAACAAAGGCAGATTCCCGA 3009 chr7 ENST00000265441.7 WNT2 AATTCAAAAATTGACTATGGGATCAAATTTGCTCGAGCAAATTTGATCCCATAGTCAA 3010 chr7 ENST00000265441.7 WNT5A AATTCAAAAACTCCCAGGACCCGCTTATTTACTCGAGTAAATAAGCGGGTCCTGGGAG 3011 chr3 ENST00000264634.8 WNT5A AATTCAAAAACAAAGAATGCCAGTATCAATTCTCGAGAATTGATACTGGCATTCTTTG 3012 chr3 ENST00000264634.8 WNT5A AATTCAAAAACCTGTTCAGATGTCAGAAGTACTCGAGTACTTCTGACATCTGAACAGG 3013 chr3 ENST00000264634.8 WNT7A AATTCAAAAACATAGGAGAAGGCTCACAAATCTCGAGATTTGTGAGCCTTCTCCTATG 3014 chr3 ENST00000285018.4 WNT7A AATTCAAAAAGGCGCAAGCATCATCTGTAACCTCGAGGTTACAGATGATGCTTGCGCC 3015 chr3 ENST00000285018.4 WNT7A AATTCAAAAATCTTCGGGAAGGAGCTCAAAGCTCGAGCTTTGAGCTCCTTCCCGAAGA 3016 chr3 ENST00000285018.4 XCL1 AATTCAAAAAGCTGTGACAATGGCAACAATTCTCGAGAATTGTTGCCATTGTCACAGC 3017 chr1 ENST00000367818.3 XCL1 AATTCAAAAATTCAACTTGTCTCTATAATAGCTCGAGCTATTATAGAGACAAGTTGAA 3018 chr1 ENST00000367818.3 XCL1 AATTCAAAAAAGATTCTGGCTAGTGTCTATCCTCGAGGATAGACACTAGCCAGAATCT 3019 chr1 ENST00000367818.3 XCL2 AATTCAAAAAACTGCCAGTTAGCAGAATCAACTCGAGTTGATTCTGCTAACTGGCAGT 3020 chr1 ENST00000367819.2 XCL2 AATTCAAAAAGTAGGGAGTGAAGTCTCACATCTCGAGATGTGAGACTTCACTCCCTAC 3021 chr1 ENST00000367819.2 XCL2 AATTCAAAAAGAAATCCAACACCAGAAATAACTCGAGTTATTTCTGGTGTTGGATTTC 3022 chr1 ENST00000367819.2 ZFP36 AATTCAAAAAGATCCGACCCTGATGAATATGCTCGAGCATATTCATCAGGGTCGGATC 3023 chr19 ENST00000597629.1 ZFP36 AATTCAAAAAATCTGTCTCCTAGAATCTTATCTCGAGATAAGATTCTAGGAGACAGAT 3024 chr19 ENST00000597629.1 ZFP36 AATTCAAAAACCCTTTATTTATGACGACTTTCTCGAGAAAGTCGTCATAAATAAAGGG 3025 chr19 ENST00000597629.1

Example 16—Method of Making and Testing Cells Deficient in Specific Cytokine Expression Using Protein Expression Blockers (PEBL)—CAR19-GM-CSF PEBL

Inject tumor in SCID-Beige mice (3e6 Raji containing Luciferase) if performing in vivo CRS experiment. This should be completed 3 weeks prior to infusion of CAR-T into mice.

The following sERteps may be taken to provide CRS resistance. A selectable marker is required to enrich for this gene modification as cytokines are secreted proteins, thus. This example describes the making of a cell CAR19-GM-CSF PEBL, in which blockade of GM-CSF secretion mitigates risk of CRS. As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Step 1: T Cell Activation (Day 0)

Purify T cells from leukapheresis chamber using Miltenyi juman PanT isolation kit. Resuspend in media. Count cells. Determine number of human T cell activation CD3/CD28 beands required to obtain 3:1 bead:cell ratio. Wash beads 2× with T cell media. Dilute cells at 1.256 cells/mL in hXcyte media. Add human T cell activation CD3/CD28 beads. Aliquot 4 ml/well of 1.256 cells/mL solution into 6-well plate. Incubate at 37° C.

Step 2: Transduction of T Cells with PEBL CAR (Day 1)

T cells are transduced with a CAR targeted to (i.e., that recognizes) one or more antigen or protein targets, for example with a Lentivirus containing a CAR construct targeting CD19, combined with the anti-GM-CSF PEBL. Expression from a polycistronic vector is preferable, allowing CD34 expression to mark both CAR and PEBL expression. However, expression can be achieved with the same viral vector expressing both the CAR and PEBL individually, or as independent transductions with separate vectors containing CAR and PEBL. Any other suitable method of transduction may be used, for example, AAV, retrovirus, etc, or through direct insertion of the CAR PEBL complex into a targeted location of the genome using homology directed repair and a donor vector containing the construct.

Step 3: Assessment of Td Efficiency (Day 10)

Take 5×10⁵ cells from each sample and analyze by flow cytometry. Wash samples with RB. Add 3 μL of anti-CD34 PE antibody. Add 5 μL of CD3 APC and 2 μL of anti-FAB BV421 (detects CAR transduction). Wash. Perform flow cytometry. Cells should be CD34-positive indicating expression of CAR and PEBL from a polycistronic vector. Harvest T cells (Day 11).

Purification of CAR-T cells. CAR+(CD34+) and GC-CSF deficient (PEBL+) cells can be enriched using a CD34-positive selection on the Miltenyi Automacs. This enriches the GC-CSF suppressed cells and enriches CAR+ cells.

Step 4: Assessment of CAR-T Activity

Inject 3×10⁷ CAR-T cells per mouse I.P. Assess serum cytokine levels. (Day 12, Day 13, Day 14). Measure serum cytokine levels using Luminex multiplex profiling assay to check for elevations in CRS-related cytokines. Perform a 4-hour chromium release assay against target cells (Raji) to assess in vitro activity (Day 11).

PEBL constructs targeting GM-CSF are provided in FIG. 6 and Tables 17 and 18.

TABLE 17 Anti-GM-CSF PEBL Constructs (SEQ ID NOS 3071-3076, respectively) ER-Retention CD28 Leader V_(L) Linker V_(H) Domain 2a trCD34 MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG EQKLISEEDLKD LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL EL (SEQ ID (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS NO: 3028) NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA LVIYYDSNRPS PGKGLEWVSN GIPERFSGSNS IWRGPYIYYA GNTATLTISGT DSVKGRFTIS QAEDEADYYCQ RDNSKNTLYL SRTQTTIVFGG QMNSLRAEDT GTKLTVLGQ AVYYCARFQG (SEQ ID YGGGFDYWGQ NO: 3026) GTLVTVSS (SEQ ID NO: 3027) MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG (GGGGS)₄AEK LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL DEL (SEQ ID (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS NO: 3029) NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA LVIYYDSNRPS PGKGLEWVSN GIPERFSGSNS IWRGPYIYYA GNTATLTISGT DSVKGRFTIS QAEDEADYYCQ RDNSKNTLYL SRTQTTIVFGG QMNSLRAEDT GTKLTVLGQ AVYYCARFQG (SEQ ID YGGGFDYWGQ NO: 3026) GTLVTVSS (SEQ ID NO: 3027) MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG TTTPAPRPPTPA LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL PTIASQPLSLRP (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS EACRPAAGGAVH NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA TRGLDFACDIYI LVIYYDSNRPS PGKGLEWVSN WAPLAGTCGVLL GIPERFSGSNS IWRGPYIYYA LSLVITLYCNHR GNTATLTISGT DSVKGRFTIS NLYKYKSRRSFI QAEDEADYYCQ RDNSKNTLYL DEKKMP SRTQTTIVFGG QMNSLRAEDT (SEQ ID GTKLTVLGQ AVYYCARFQG NO: 3030) (SEQ ID YGGGFDYWGQ NO: 3026) GTLVTVSS (SEQ ID NO: 3027) MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG EQKLISEEDLKD GSGATNFSLLK MPRGWTALCLL LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL EL (SEQ ID QAGDVEENPGP SLLPSGFMSLD (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS NO: 3028) (SEQ ID NNGTATPELPT NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA NO: 3031) QGTFSNVSTNV LVIYYDSNRPS PGKGLEWVSN SYQETTTPSTL GIPERFSGSNS IWRGPYIYYA GSTSLHPVSQH GNTATLTISGT DSVKGRFTIS GNEATTNITET QAEDEADYYCQ RDNSKNTLYL TVKFTSTSVIT SRTQTTIVFGG QMNSLRAEDT SVYGNTNSSVQ GTKLTVLGQ AVYYCARFQG SQTSVISTVFT (SEQ ID YGGGFDYWGQ TPANVSTPETT NO: 3026) GTLVTVSS LKPSLSPGNVS (SEQ ID DLSTTSTSLAT NO: 3027) SPTKPYTSSSP ILSDIKAEIKC SGIREVKLTQG ICLEQNKTSSC AEFKKDRGEGL ARVLCGEEQAD ADAGAQVCSLL LAQSEVRPQCL LLVLANRTEIS SKLQLMKKHQS DLKKLGILDFT EQDVASHQSYS QKTLIALVTSG ALLAVLGITGY FLMNRRSWSPI (SEQ ID NO: 3032) MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG (GGGGS)₄AEK GSGATNFSLLK MPRGWTALCLL LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL DEL (SEQ ID QAGDVEENPGP SLLPSGFMSLD (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS NO: 3029) (SEQ ID NNGTATPELPT NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA NO: 3031) QGTFSNVSTNV LVIYYDSNRPS PGKGLEWVSN SYQETTTPSTL GIPERFSGSNS IWRGPYIYYA GSTSLHPVSQH GNTATLTISGT DSVKGRFTIS GNEATTNITET QAEDEADYYCQ RDNSKNTLYL TVKFTSTSVIT SRTQTTIVFGG QMNSLRAEDT SVYGNTNSSVQ GTKLTVLGQ AVYYCARFQG SQTSVISTVFT (SEQ ID YGGGFDYWGQ TPANVSTPETT NO: 3026) GTLVTVSS LKPSLSPGNVS (SEQ ID DLSTTSTSLAT NO: 3027) SPTKPYTSSSP ILSDIKAEIKC SGIREVKLTQG ICLEQNKTSSC AEFKKDRGEGL ARVLCGEEQAD ADAGAQVCSLL LAQSEVRPQCL LLVLANRTEIS SKLQLMKKHQS DLKKLGILDFT EQDVASHQSYS QKTLIALVTSG ALLAVLGITGY FLMNRRSWSPI (SEQ ID NO: 3032) MALPVTALLLP DIELTQPPSVS GGGGS(n)n = QVQLVESGGG TTTPAPRPPTPA GSGATNFSLLK MPRGWTALCLL LALLLHAARP VAPGQTARISC 1, 2, 3, 4 LVQPGGSLRL PTIASQPLSLRP QAGDVEENPGP SLLPSGFMSLD (SEQ ID SGDNLPGKYVH (SEQ ID SCAASGFTFS EACRPAAGGAVH (SEQ ID NNGTATPELPT NO: 1) WYQQKPGQAPV NO: 3069) SHWMSWVRQA TRGLDFACDIYI NO: 3031) QGTFSNVSTNV LVIYYDSNRPS PGKGLEWVSN WAPLAGTCGVLL SYQETTTPSTL GIPERFSGSNS IWRGPYIYYA LSLVITLYCNHR GSTSLHPVSQH GNTATLTISGT DSVKGRFTIS NLYKYKSRRSFI GNEATTNITET QAEDEADYYCQ RDNSKNTLYL DEKKMP TVKFTSTSVIT SRTQTTIVFGG QMNSLRAEDT (SEQ ID NO:  SVYGNTNSSVQ GTKLTVLGQ AVYYCARFQG 3030) SQTSVISTVFT (SEQ ID YGGGFDYWGQ TPANVSTPETT NO: 3026) GTLVTVSS LKPSLSPGNVS (SEQ ID DLSTTSTSLAT NO: 3027) SPTKPYTSSSP ILSDIKAEIKC SGIREVKLTQG ICLEQNKTSSC AEFKKDRGEGL ARVLCGEEQAD ADAGAQVCSLL LAQSEVRPQCL LLVLANRTEIS SKLQLMKKHQS DLKKLGILDFT EQDVASHQSYS QKTLIALVTSG ALLAVLGITGY FLMNRRSWSPI (SEQ ID NO: 3032)

TABLE 18 CD19 CAR with GM-CSF PEBL Constructs (SEQ ID NOS 3077-3082, respectively)

CD8a CD19 CD19 CD8a CD2 CD28 CD8a

Leader V_(H) Linker V_(L) Hinge 8tm Co-stim CD3z 2a Leader V_(L) Linker V_(H)

2a Tag MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG EQKLISEE ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG DLKDEL ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA (SEQ ID ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH NO: 3028) (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS NO: 3033) NO: 3038) NO: 3026) (SEQ ID NO: 3027) MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG (GGGGS)₄ ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG AEKDEL ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA (SEQ ID ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH NO: 3029) (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS NO: 3033) NO: 3038) NO: 3026) (SEQ ID NO: 3027) MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG TTTPAPRP ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG PTPAPTIA ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA SQPLSLRP ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH EACRPAAG (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA AAVHTRGL NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV DFACDIYI HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY WAPLAGTC GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK GVLLLSLV LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD ITLYCNHR DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL NLYKYKSR GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE RSFIDEKK GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA MP ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG (SEQ ID FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT NO: 3030) (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS NO: 3033) NO: 3038) NO: 3026) (SEQ ID NO: 3027) MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG EQKLISEE GSGATN MPRGWTA ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG DLKDEL FSLLKQ LCLLSLL ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA (SEQ ID AGDVEE PSGFMSL ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH NO: 3028) NPGP DNNGTAT (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA (SEQ PELPTQG NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV ID NO: TFSNVST HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY 3031) NVSYQET GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK TTPSTLG LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD STSLHPV DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL SQHGNEA GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE TTNITET GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA TVKFTST ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG SVITSVY FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT GNTNSSV (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS QSQTSVI NO: 3033) NO: 3038) NO: 3026) (SEQ ID STVFTTP NO: 3027) ANVSTPE TTLKPSL SPGNVSD LSTTSTS LATSPTK PYTSSSP ILSDIKA EIKCSGI REVKLTQ GICLEQN KTSSCAE FKKDRGE GLARVLC GEEQADA DAGAQVC SLLLAQS EVRPQCL LLVLANR TEISSKL QLMKKHQ SDLKKLG ILDFTEQ DVASHQS YSQKTLI ALVTSGA LLAVLGI TGYFLMN RRSWSPI (SEQ ID NO: 10) MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG (GGGGS)₄ GSGATN MPRGWTA ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG AEKDEL FSLLKQ LCLLSLL ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA (SEQ ID AGDVEE PSGFMSL ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH NO: 3029) NPGP DNNGTAT (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA (SEQ PELPTQG NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV ID NO: TFSNVST HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY 3031) NVSYQET GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK TTPSTLG LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD STSLHPV DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL SQHGNEA GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE TTNITET GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA TVKFTST ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG SVITSVY FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT GNTNSSV (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS QSQTSVI NO: 3033) NO: 3038) NO: 3026) (SEQ ID STVFTTP NO: 3027) ANVSTPE TTLKPSL SPGNVSD LSTTSTS LATSPTK PYTSSSP ILSDIKA EIKCSGI REVKLTQ GICLEQN KTSSCAE FKKDRGE GLARVLC GEEQADA DAGAQVC SLLLAQS EVRPQCL LLVLANR TEISSKL QLMKKHQ SDLKKLG ILDFTEQ DVASHQS YSQKTLI ALVTSGA LLAVLGI TGYFLMN RRSWSPI (SEQ ID NO: 10) MALPVT DIQMTQTTS GGGGS₄ EVKLQEQGP TTTPAPRPP FWVLVVVGG RSKRSRLLH RVKFSRSA GSGATNFS MALPVT DIELQTPP GGGG QVQLVESG TTTPAPRP GSGATN MPRGWTA ALLLPL SLSASLGDR (SEQ ID GLVAPSQSL TPAPTIASQ VLACYSLLV SDYMNMTPR DAPAYKQG LLKQAGDV ALLLPL SVSVAPGQ S(n)= 1, GGLVQPGG PTPAPTIA FSLLKQ LCLLSLL ALLLHA VTISCRASQ NO: 9) SVTCTVSGV PLSLRPEAC TVAFIIFWV RPGPTRKHY QNQLYNEL EENPGP ALLLHA TARISCSG 2, 3, 4 SLRLSCAA SQPLSLRP AGDVEE PSGFMSL ARP DISKYLNWY SLPDYGVSW RPAAGGAVH (SEQ ID QPYAPPRDF NLGRREEY (SEQ ID ARP DNLPGKYV (SEQ ID SGFTFSSH EACRPAAG NPGP DNNGTAT (SEQ ID QQKPDGTVK IRQPPRKGL TRGLDFACD NO: 3036) AAYRS DVLDKRRG NO: 3031) (SEQ ID HWYQQKPG NO: 3069) WMSWVRQA AAVHTRGL (SEQ PELPTQG NO: 1) LLIYHTSRL EWLGVIWGS (SEQ ID (SEQ ID RDPEMGGK NO: 1) QAPVLVIY PGKGLEWV DFACDIYI ID NO: TFSNVST HSGVPSRFS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE YDSNRPSG SNIWRGPY WAPLAGTC 3031) NVSYQET GSGSGTDYS KSRLTIIKD GLYNELQK IPERFSGS IYYADSVK GVLLLSLV TTPSTLG LTISNLEQE NSKSQVFLK DKMAEAYS NSGNTATL GRFTISRD ITLYCNHR STSLHPV DIATYFCQQ MNSLQTDDT EIGMKGER TISGTQAE NSKNTLYL NLYKYKSR SQHGNEA GNTLPYTFG AIYYCAKHY RRGKGHDG DEADYYCQ QMNSLRAE RSFIDEKK TTNITET GGTKLEITR YYGGSYAMD LYQGLSTA SRTQTTIV DTAVYYCA MP TVKFTST ADAAPTVSI YWGQGTSVS TKDTYDAL FGGGTKLT RFQGYGGG (SEQ ID SVITSVY FPPSSN (SEQ ID HMQALPPR VLGQ FDYWGQGT NO: 3030) GNTNSSV (SEQ ID NO: 3034) (SEQ ID (SEQ ID LVTVSS QSQTSVI NO: 3033) NO: 3038) NO: 3026) (SEQ ID STVFTTP NO: 3027) ANVSTPE TTLKPSL SPGNVSD LSTTSTS LATSPTK PYTSSSP ILSDIKA EIKCSGI REVKLTQ GICLEQN KTSSCAE FKKDRGE GLARVLC GEEQADA DAGAQVC SLLLAQS EVRPQCL LLVLANR TEISSKL QLMKKHQ SDLKKLG ILDFTEQ DVASHQS YSQKTLI ALVTSGA LLAVLGI TGYFLMN RRSWSPI (SEQ ID NO: 10)

indicates data missing or illegible when filed

Example 17—In Vitro CRS Assay for Testing Efficacy of Inducing CRS after Deletion of GM-CSF in CART19

Cell lines: CD19 positive B-ALL cell line RAMOS was used to evaluate CRS in an in vitro assay. Prior to assay, RAMOS cells were stably transfected with GFP using lentiviral transduction and cultured in RPMI+10% FBS+ Pen/Strep.

Isolation of normal donor monocytes and T cells: Primary human T cells and monocytes were isolated from normal healthy human donors. T cell cells were isolated from PBMC using CD4+CD8+ selection (Miltenyi Biotec) and monocytes were separated using Miltenyi biotec classical Monocyte Isolation beads according to the manufactures protocol.

T cell culture and CAR-T gene editing: T cells were subsequently resuspended at a concentration of 1×10⁶ cells/mL in Xcyte media supplemented with 50 U/mL IL-2 and 10 ng/ml IL-15 in the presence of anti-CD3/CD28 beads (Bead to cell ratio 3:1). Twenty-four hours after initial stimulation, T cells were transfected with lentiviral vector encoding the CD19 CAR construct in the presence of polybrene (final conc. 6 μg/ml). Stimulatory beads were removed on day 2. CART19 cells were suspended at 4×10⁶ T cells were electroporated in 100 μl buffer P3 with 15 μg spCas9 mRNA (Trilink CA.) and 20 μg of GM-CSF gRNA (Trilink) using a nucleofector 4D, program EO-115. Control CAR19 T cells were electroporated without GM-CSF gRNA. T-cells were subsequently evaluated at day 6 for CD34 (bicistronic marker of CAR-T) and intracellular GM-CSF expression using flowcytometry prior to co-culture assay.

Production of monocyte lineage cells: For iDC generation, monocytes (1×10⁶) were plated in 6 mLs of RPMI 1640 supplemented with supplemented with 0.1 mmol/L MEM Non-Essential Amino Acids, 2 mmol/L L-glutamine, 100 units/mL penicillin, 100 μg/mL streptomycin (Life Technologies) and 10% fetal calf serum (cR10). cR10 was subsequently supplemented with 0.2 μg/mL human IL-4 (Peptotec) and 0.2 μg/mL GM-CSF (Peptotec).

For macrophage and activated macrophage generation cR10 was supplemented with 10% human A/B serum instead of fetal calf serum (hR10). For activated macrophages hR10 medium was supplemented with 30 ng/ml of LPS. On day 4 cytokines and LPS were replenished. Macrophages, activated macrophages and iDC were harvested using 2 mmol/L EDTA (immature dendritic cells) on day 6 post-isolation. Twenty-four hours later, cells were harvested with 2 mmol/L EDTA and stained with CD45, CD80 and CD86 to confirm immature DC and mature DC differentiation.

Co-culture assay: CAR-T cells were combined at the following ratios in 200 ul per 96 well: 12.5K UCART-19 (with or with-out GM-CSF KO), Target, 50K Ramos cells (CD19+) and monocyte derived cells, 1K iDC or 5K macrophages or 5K activated macrophages.

Co-cultures were subsequently incubated for at 37° C. and 100 ul of assay supernatant was collected at 24 hr and 48 hr for cytokine analysis.

Measurement of Cytokine Levels

Cytokine concentration determination from culture supernatants was performed using IL-6 ELISA plate (R&D systems). Prior to analysis supernatant's were centrifuged at 300 g for 10 mins at 4° C. and subsequently diluted 1:10 in assay calibrator diluent. Measurements were performed using standard product protocols.

GM-CSF deficient CART19 induced significantly lower il-6 expression across the different monocyte lineages. FIGS. 8 and 10

Example 18—In Vitro CRS Assay for Testing Efficacy of Inducing CRS after Deletion of GM-CSF in T Cells

Isolation of normal donor monocytes and T cells: Primary human T cells and monocytes were isolated from normal healthy human donors. T cell cells were isolated from PBMC using CD4+CD8+ selection (Miltenyi Biotec) and monocytes were separated using Miltenyi Biotec classical Monocyte Isolation beads according to the manufactures protocol.

T cell culture and gene editing: T cells were subsequently resuspended at a concentration of 106 cells/mL in Xcyte media supplemented with 50 U/mL IL-2 and 10 ng/ml IL-15 in the presence of anti-CD3/CD28 beads (Bead to cell ratio 3:1) (Life Technologies, catalog #111.32D). Twenty-four hours after initial stimulation. Stimulatory beads were removed on day 2.4×10⁶ T cells were electroporated in 100 μl buffer P3 with 15 μg spCas9 mRNA (Trilink CA.) and 20 μg of TRAC gRNA (Trilink) using a nucleofector 4D, program EO-115. Control CAR19 T cells were electroporated without GM-CSF gRNA. T-cells were subsequently evaluated at day 6 for GM-CSF expression prior to co-culture assay using flowcytometry.

Production of monocyte lineage cells: For iDC generation, monocytes (1×10⁶) were plated in 6 mLs of RPMI 1640 supplemented with supplemented with 0.1 mmol/L MEM Non-Essential Amino Acids, 2 mmol/L L-glutamine, 100 units/mL penicillin, 100 μg/mL streptomycin (Life Technologies) and 10% fetal calf serum (cR10). cR10 was subsequently supplemented with 0.2 μg/mL human IL-4 (Peptotec) and 0.2 μg/mL GM-CSF (Peptotec). On day 4 cytokines and LPS were replenished. iDC were harvested using 2 mmol/L EDTA (immature dendritic cells) on day 6 post-isolation.

Co-culture assay: T cells were combined at the following ratios in 200 ul per 96 well: 12.5K T cells (with or with-out GM-CSF KO), 50K anti-CD3/CD28 beads and 1K iDC Co-cultures were subsequently incubated for at 37° C. and 100 ul of assay supernatant was collected at 24 hr and 48 hr for cytokine analysis.

Measurement of cytokine levels: Cytokine concentration determination from culture supernatants was performed using IL-6 ELISA plate (R&D systems). Prior to analysis supernatants were centrifuged at 300×g for 10 mins at 4° C. and subsequently diluted 1:10 in assay calibrator diluent. Measurements were performed using standard product protocols.

Deletion of GM-CSF reduced IL-6 production >3-fold at 24 hrs (FIGS. 7 and 8 ) and >4-fold at 48 hrs (FIGS. 9 and 10 ) relative to non-edited T cells.

GM-CSF deficient T cells induced significantly lower IL-6 expression across the different monocyte lineages.

Example 19—Method for Making and Testing a Genome-Edited CAR-T Cell Deficient at Inducing CRS by Insertion of Selectable Marker into Gene Edited Locus

Inject primary B-ALL (2×10⁶) in NSG mice if performing an in vivo CRS experiment. This should be completed 3 weeks prior to infusion of CAR-T into mice.

The following steps may be taken to provide a genome-edited, CRS-resistant, CAR-T cells. This example describes the making of a CD19CARTΔGMCSFΔCD38 mutant IL-7R T cell, in which the deletion of GM-CSF mitigates risk of CRS, deletion of CD3e prevent TCR signaling and GvHD and the mutant IL-7R enhances proliferation of the CAR-T sufficiently to induce CRS in this model. Sequences encoding a mutant, constitutively active IL-7R sequence can be found in Table 19, or found in the art. As those of skill in the art will recognize, certain of the steps may be conducted sequentially or out of the order listed below, though perhaps leading to different efficiency.

Step 1: T Cell Activation (Day 0)

Purify T cells from a leukapheresis chamber using a Miltenyi human PanT isolation kit. Resuspend in media. Count cells. Determine the number of human T cell activation CD3/CD28 beads required to obtain a 3:1 bead:cell ratio. Wash beads 2× with T cell media. Dilute cells at 1.256 cells/mL in hXcyte media. Add human T cell activation CD3/CD28 beads. Aliquot 4 mL/well of 1.256 cell/mL solution into a 6 well plate. Incubate cells at 37° C.

Step 2: T Cell Transduction (Day 1)

CAR-T cells may then be transduced with one or more CARs targeted to (i.e., that recognizes) one or more targets, for example with a lentivirus containing a CAR construct. Any other suitable method of transduction may be used.

Step 3: CRISPR (Day 2)

In a CRS-resistant CAR-T cell, cytokine/chemokine/transcription factor genes or transcription factors may be deleted to prevent secretion of factors that induce secretion of cytokines from myeloid cells. Deletion may be accomplished by electroporating with Cas9 mRNA and gRNA against the target(s). Other techniques, however, could be used to suppress expression of the target. These include other genome editing techniques such as TALENs, RNA interference, and eliciting of internal binding of the antigen to prevent cell surface expression. Examples of gRNAs that may be used include those shown in Tables 8-10, and others known in the art.

Nuecleofection Sample ID gRNA#1 gRNA#2 Cas9 Buffer P3 UCART19 20 μg 20 μg gCD3ε 15 μg Cas9 100 μl gGM-CSF mRNA

Cells are harvested, isolated, and purified, for example using magnetic selection with a labelled antibody-coated magnetic beads that bind to a cell-specific protein (available from, e.g., Miltenyi Biotec). For T cells, anti-CD3/CD28 beads could be used. Other purification techniques are known in the art and could be used.

TABLE 19 Sequences or Constitutively Expressing IL-7R Trucated Trucated CD8a CD19 CD19 CD8a CD28 Truncated IL-7R IL-7 IL-7R Leader V_(L) Linker V_(H) Hinge CD28tm Co-stim CD3z 2a CD34 ECD TMD ICD Description MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC YREGANDFV LLTCPTISI KKRIKPIVW IL7R with L5 and L6 ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF VTFNTSHLQ LSFFSVALL PSLPDHKKT elbows with CPT trans- ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA KKYVKVLMH VILACVLW LEHLCKKPR membrane T-ALL ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT DVAYRQEKD (SEQ ID KNLNVSFNP mutation insertion (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS ENKWTHVNL NO: 3045) ESFLDCQIH only NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST SSTKLTLLQ RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV RKLQPAAMY EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT EIKVRSIPD FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF HYFKGFWSE KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV WSPSYYFRT SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ PEINNSSGE VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV MDPI DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST (SEQ ID NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL NO: 3040) LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC YREGANDFV LLTCPTISI KKRIKPIVW IL7R with L5 and L6 ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF VTFNTSHLQ LSFFSVALL PSLPDHKKT elbows with CPT trans- ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA KKYVKVLMH VILACVLW LEHLCKKPR membrane T-ALL ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT DVAYRQEKD (SEQ ID KNLNVSFNP mutation insertion (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS ENKWTHVNL NO: 3045) ESFLDCQIH and S185C B-ALL NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST SCTKLTLLQ RVDDIQARD mutation YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV RKLQPAAMY EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT EIKVRSIPD FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF HYFKGFWSE KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV WSPSYYFRT SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ PEINNSSGE VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV MD DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST (SEQ ID NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL NO: 3041) LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC YREGANDFV LLTISILS KKRIKPIVW IL7R with L5 and L6 ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF VTFNTSHLQ FFSVALLV PSLPDHKKT elbows with S185C ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA KKYVKVLMH ILACVLW LEHLCKKPR B-ALL mutation only ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT DVAYRQEKD (SEQ ID KNLNVSFNP (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS ENKWTHVNL NO: 3046) ESFLDCQIH NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST SCTKLTLLQ RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV RKLQPAAMY EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT EIKVRSIPD FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF HYFKGFWSE KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV WSPSYYFRT SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ PEINNSSGE VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV MD DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST (SEQ ID NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL NO: 3041) LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC YREGANDFV LLTISILSF KKRIKPIVW IL7R with L5 and L6 ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF VTFNTSHLQ FSVALLVIL PSLPDHKKT elbows WT ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA KKYVKVLMH ACVLW LEHLCKKPR ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT DVAYRQEKD (SEQ ID KNLNVSFNP (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS ENKWTHVNL NO: 46) ESFLDCQIH NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST SSTKLTLLQ RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV RKLQPAAMY EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT EIKVRSIPD FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF HYFKGFWSE KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV WSPSYYFRT SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ PEINNSSGE VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV MDPI DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST (SEQ ID NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL NO: 3040) LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC VNLSSTKLT LLTCPTISI KKRIKPIVW IL7R with L6 elbow ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF LLQRKLQPA LSFFSVALL PSLPDHKKT only with CPT trans- ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA AMYEIKVRS VILACVLW LEHLCKKPR membrane T-ALL ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT IPDHYFKGF (SEQ ID KNLNVSFNP mutation insertion (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS WSEWSPSYY NO: 3045) ESFLDCQIH only NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST FRTPEINNS RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV SGEMDPI EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT (SEQ ID FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF NO: 3042) KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC VNLSCTKLT LLTCPTISI KKRIKPIVW IL7R with L6 elbows ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF LLQTKLQPA LSFFSVALL PSLPDHKKT with CPT trans- ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA AMYEIKVRS VILACVLW LEHLCKKPR membrane T-ALL ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT IPDHYFKGF (SEQ ID KNLNVSFNP mutation insertion (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS WSEWSPSYY NO: 3045) ESFLDCQIH and S185C B-ALL NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST FRTPEINNS RVDDIQARD mutation YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV SGEMDPI EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT (SEQ ID FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF NO: 3043) KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC VNLSCTKLT LLTISILSF KKRIKPIVW IL7R with L6 elbows ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF LLQTKLQPA FSVALLVIL PSLPDHKKT with S185C B-ALL ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA AMYEIKVRS ACVLW LEHLCKKPR mutation only ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT IPDHYFKGF (SEQ ID KNLNVSFNP (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS WSEWSPSYY NO: 3046) ESFLDCQIH NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST FRTPEINNS RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV SGEMDPI EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT (SEQ ID FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF NO: 3043) KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC VNLSSTKLT LLTISILSF KKRIKPIVW IL7R with L6 elbows ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF LLQRKLQPA FSVALLVIL PSLPDHKKT WT ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA AMYEIKVRS ACVLW LEHLCKKPR ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT IPDHYFKGF (SEQ ID KNLNVSFNP (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS WSEWSPSYY NO: 3046) ESFLDCQIH NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST FRTPEINNS RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV SGEMDPI EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT (SEQ ID FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF NO: 3042) KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039) MALPVT DIQMTQTT GGGGS₄ EVKLQESGP TTTPAPRPP FWVLVVVG RSKRSRLLH RVKFSRSA GSGATNFS MPRGWTALC PEINNSSGE LLTCPTISI KKRIKPIVW IL-7R with CPT T-ALL ALLLPL SSLSASLG (SEQ ID GLVAPSQSL TPAPTIASQ GVLACYSL SDYMNMTPR DAPAYKQG LLKQAGDV LLSLLPSGF MDPI LSFFSVALL PSLPDHKKT mutation. Lacking ALLLHA DRVTISCR NO: 9) SVTCTVSGV PLSLRPEAC LVTVAFII RPGPTRKHY QNQLYNEL EENPGP MSLDNNGTA (SEQ ID VILACVLW LEHLCKKPR elbows and WSEWS ARP ASQDISKY SLPDYGVSW RPAAGGAVH FWV QPYAPPRDF NLGRREEY (SEQ ID TPELPTQGT NO: 3044) (SEQ ID KNLNVSFNP (SEQ ID NO: 3070) (SEQ ID LNWYQQKP IRQPPRKGL TRGLDFACD (SEQ ID AAYRS DVLDKRRG NO: 3031) FSNVSTNVS NO: 3045) ESFLDCQIH motif (sugar bridge) NO: 1) DGTVKLLI EWLGVIWGS (SEQ ID NO: 3036) (SEQ ID RDPEMGGK YQETTTPST RVDDIQARD YHTSRLHS ETTYYNSAL NO: 3035) NO: 3037) PRRKNPQE LGSTSLHPV EVEGFLQDT GVPSRFSG KSRLKSRLT GLYNELQK SQHGNEATT FPQQLEESE SGSGTDYS IIKDNSKSQ DKMAEAYS NITETTVKF KQRLGGDVQ LTISNLEQ VFLKMNSLQ EIGMKGER TSTSVITSV SPNCPSEDV QGNTLPYT TDDTAIYYC RRGKGHDG YGNTNSSVQ VITPESFGR FGGGTKLE AKHYYYGGS LYQGLSTA SQTSVISTV DSSLTCLAG ITRADAAP YAMDYWGQG TKDTYDAL FTTPANVST NVSACDAPI TVSIFPPS TSVTVSS HMQALPPR PETTLKPSL LSSSRSLDC SN (SEQ ID (SEQ ID LPSNVSDLS RESGKNGPH (SEQ ID NO: 3034) NO: 3038) TTSTSLATS VYQDLLLSL NO: 3033) PTKPYTSSS GTTNSTLPP PILSDIKAE PFSLQSGIL IKCSGIREV TLNPVAQGQ KLTQGICLE PILTSLGSN QNKTSSCAE QEEAYVTMS FKKDRGEGL SFYQNQ ARVLCGEEQ (SEQ ID ADADAGAQV NO: 3047) CSLLLAQSE VRPQCLLLV LANRTEISS KLQLMKKHQ SDLKKLG (SEQ ID NO: 3039)

Protocol—Nucleofection Using Nucleofector 4D:

Perform nucleofection protocol as described above (Example 6), using 20 μg of each gRNA (gGM-CSF and gCD38) to each tube of 15 μg Cas9 mRNA.

Step 4: Assessment of CRISPR Activity and Td Efficiency (Day 10)

Take 5×10⁵ cells from each sample and analyze by flow cytometry. Wash samples with RB. Add 5 μl of CD3 APC and 2 μl of anti-FAB BV421 (detects CAR transduction). Wash. Perform Flow cytometry. Cells should be CD38-negative, CD34-positive and FAB+. Harvest T cells (Day 11).

Purification of CAR-T cells. TCR negative cells can be purified using TCRa/b negative selection to remove TCR positive cells.

Step 5: Assessment of CAR-T Activity In Vivo

Inject 5×10⁶ CAR-T per mouse I.V. Assess serum cytokine levels (Day +1, +2, +3 +4, +5, +10, +15). Measure serum cytokine levels using Luminex multiplex cytokine profiling assay to check for elevations in CRS related cytokines. Perform a 4-hr chromium release assay against targets cells (Raji) to assess in vitro activity (Day 11). Monitor efficacy of tumor clearance using flow cytometry of blood to detect hCD45, CD19+ cells.

A modified gRNA protocol for T cell CRISPR and CAR-T transduction of UCART19 is provided below.

Day 0—T Cell Activation:

Purify T cells from a leukapheresis chamber using a Miltenyi human PanT isolation kit. Resuspend in media. Count cells. Determine the number of human T cell activation CD3/CD28 beads required to obtain a 3:1 bead:cell ratio. Wash beads 2× with T cell media. Dilute cells at 1.256 cells/mL in hXcyte media. Add human T cell activation CD3/CD28 beads

T cells may then be transduced with one or more CARs targeted to (i.e., that recognizes) one or more targets, for example with a lentivirus containing a CAR construct. Any other suitable method of transduction may be used.

Day 2: 4×10⁶ cells per reaction are used. EO-115-100 μl transfection volume is programmed, and the entire supplement added to the Nucleofector™ Solution P3. Cell culture plates are prepared by filling appropriate number of wells with desired volume of recommended culture media (2 ml in 6 well plate) and pre-incubating/equilibrating plates in a humidified 37° C./5% CO₂ incubator. Beads are magnetically removed (twice to ensure complete removal), then cells counted and cell density determined. The required number of cells are centrifuged at 90×g for 10 minutes at room temperature, the supernatant removed completely. Cells are then resuspended in PBS (1 ml) and transferred to a microcentrifuge tube, and the required number of cells centrifuged at 90×g for 10 minutes at room temperature. The supernatant is removed completely, and the cell pellet resuspended carefully in complete room temperature 4D Nucleofector™ Solution P3, 4×10⁶ per 100 μl). Twenty μg of gRNA (gGM-CSF and gTRAC) are added to each tube of 15 μg Cas9 mRNA. Then 100 μl of cells is added to each tube of Cas9/gRNA, gently mixed and everything transferred into the Nucleocuvette™. The cuvette is gently tapped to remove bubbles. Electroporation is carried out using program (Human T cell stim EO-115). After run completion, the Nucleocuvette™ is carefully removed from the vessel from the retainer using a specialized tool. Cells are resuspended with pre-warmed medium. The media is then taken up from destination well, added to cuvette, and gently pipetted up and down two to three times. This is then transferred to well. This procedure is repeated with media from same well and incubated at 37° C.

Day 5: Assessment of CRISPR activity and Td efficiency. Samples of cells may then be assessed for transduction efficiency by taking a 5×10⁵ cells from each sample and analyzing by flow cytometry. Samples are fix permeabilised and analysed by FACS for CD3, CD34 and intracellular GM-CSF.

Assessment of Genetic Deletion.

To assess genetic deletion of GM-CSF and TRAC, 5×10⁵ cells are harvested from each sample and their DNA extracted. Gene editing efficiency is assessed using target sequencing of the target loci using TIDE-analysis or deep sequencing.

Day 11

Bleed mice and measure tumor burden.

CD3 deplete T cells and inject into mice.

Inject mice with 5×10⁶ CAR+ T cells/mouse.

Mouse groups are provided in Table 20 below:

TABLE 20 Sample Gene T cell ID editing Tumor source CAR-T CAR-T A — 2 × 10⁶/ — — mouse B TRAC 2 × 10⁶/ PanT CAR19 + 5 × 10⁶/ mouse CD34 mouse C TRAC + 2 × 10⁶/ PanT CAR 19 5 × 10⁶/ GM-CSF mouse CD34 mouse D TRAC 2 × 10⁶/ PanT CAR 19 + 5 × 10⁶/ mouse IL7r + CD34 mouse E TRAC + 2 × 10⁶/ PanT CAR 19 + 5 × 10⁶/ GM-CSF mouse IL7r + CD34 mouse Attune - CAR-T in vivo panel - CRS Titer 50 μl blood or Bandpass 500K in Detector (nm) Antigen Colour Product # 100 μl BL1 530/30 BL2 695/40 7aad 7AAd 1 ul RL1 670/14 CD19 APC BD555415 2 ul RL2 720/30 RL3 780/60 CD4 APC-H7 BD560158 1 ul VL1 450/40 mCD45 BV421 BD563890 1 ul VL2 525/50 CD8 BV510 BD563256 4 ul VL3 610/20 VL4 660/20 CD3 BV650 BD563852 2 ul VL5 710/50

Cytokine analysis and assessment of CRS is assed using Millipore luminex multiplex cytokine analysis.

Sequences for preparation of a vector as described herein include, but are not limited to, the following:

Left ITR of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3048 CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGC GCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCT Left Homology Arm of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3049 cctgagatggatgcagccacagccctggagccagcctgaagctcctggtgtcttctgggggctacatataggagtgtagtccgaacctc agaggggcaaacctgctctgcagagggaatcaaggttcacataaccagagaggggagtcactcaggaaggtggctccagagccaagagt cagactctgggtcccgacttgacccagccacaccccctctgaagcttgctgagagtggctgcagtctcgctgctggatgtgcacatggt ggtcattccctctgctcacaggggcaggggtccccccttactggactgaggttgccccctgctccaggtcctgggtgggagcccatgtg aactgtcagtggggcaggtctgtgagagctcccctcacactcaagtctctcacagtggccagagaagaggaaggctggagtcagaatga ggcaccagggcgggcatagcctgcccaaaggcccctgggattacaggcaggatggggagccctatctaagtgtctcccacgccccaccc cagccattccaggccaggaagtccaaactgtgcccctcagagggagggggcagcctcaggcccattcagactgcccagggagggctgga gagccctcaggaaggcgggtgggtgggctgtcggttcttggaaaggttcattaatgaaaacccccaagcctgaccacctagggaaaagg ctcaccgttcccatgtgtggctgataagggccaggagattccacagttcaggtagttcccccgcctccctggcattttgtggtcaccat taatcatttcctctgtgtatttaagagctcttttgccagtgagcccaGTACACAGAGAGAAAGGCTAAAGTTCTCTGGAGGATGTGGCT GCAGAGCCTGCTGCTCTTGGGCACTGTGGCCTGCAGCATCTCTGCACCCGCCCGCTCGCCCAGCCCCAGCACGCAGCCCTGGGAGCATG TGAATGCCATCCAGGAGGCCC EFS promotor of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3050 GGCTCCGGTGCCCGTCAGTGGGCAGAGCGCACATCGCCCACAGTCCCCGAGAAGTTGGGGGGAGGGGTCGGCAATTGATCCGGTGCCTA GAGAAGGTGGCGCGGGGTAAACTGGGAAAGTGATGTCGTGTACTGGCTCCGCCTTTTTCCCGAGGGTGGGGGAGAACCGTATATAAGTG CAGTAGTCGCCGTGAACGTTCTTTTTCGCAACGGGTTTGCCGCCAGAACACAGG trCD34 of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3051 atgccgcggggctggaccgcgctttgcttgctgagtttgctgccttctgggttcatgagtcttgacaacaacggtactgctaccccaga gttacctacccagggaacattttcaaatgtttctacaaatgtatcctaccaagaaactacaacacctagtacccttggaagtaccagcc tgcaccctgtgtctcaacatggcaatgaggccacaacaaacatcacagaaacgacagtcaaattcacatctacctctgtgataacctca gtttatggaaacacaaactcttctgtccagtcacagacctctgtaatcagcacagtgttcaccaccccagccaacgtttcaactccaga gacaaccttgaagcctagcctgtcacctggaaatgtttcagacctttcaaccactagcactagccttgcaacatctcccactaaaccct atacatcatcttctcctatcctaagtgacatcaaggcagaaatcaaatgttcaggcatcagagaagtgaaattgactcagggcatctgc ctggagcaaaataagacctccagctgtgcggagtttaagaaggacaggggagagggcctggcccgagtgctgtgtggggaggagcaggc tgatgctgatgctggggcccaggtatgctccctgctccttgcccagtctgaggtgaggcctcagtgtctactgctggtcttggccaaca gaacagaaatttccagcaaactccaacttatgaaaaagcaccaatctgacctgaaaaagctggggatcctagatttcactgagcaagat gttgcaagccaccagagctattcccaaaagaccctgattgcactggtcacctcgggagccctgctggctgtcttgggcatcactggcta tttcctgatgaatcgccgcagctggagccccatttaa hGMB Poly A of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3052 ACGGGTGGCATCCCTGTGACCCCTCCCCAGTGCCTCTCCTGGCCCTGGAAGTTGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAAA TTAAGTTGCATCATTTTGTCTGACTAGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTGGTATGGAGCAAGGGGCAAGTTGGGAA GACAACCTGTAGGGCCTGCGGGGTCTATTGGGAACCAAGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCCGCCTCCTGGG TTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTTGTTGGGATTCCAGGCATGCATGACCAGGCTCAGCTAATTTTTGTTTTTTTGGTAG AGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCCAACTCCTAATCTCAGGTGATCTACCCACCTTGGCCTCCCAAATTGCTGGGATT ACAGGCGTGAACCACTGCTCCCTTCCCTGTCCTTCTGATTTTGTAGGTAACCACGTGCGGACCGA RHA of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3053 CGTCTCCTGAACCTGAGTAGAGACACTGCTGCTGAGATGgtaagtgagagaatgtgggcctgtgcctaggccacccagctggcccctga ctggccacgcctgtcagcttgataacatgacattttccttttctacagAATGAAACAGTAGAAGTCATCTCAGAAATGTTTGACCTCCA Ggtaagatgcttctctctgacatagctttccagaagcccctgccctggggtggaggtggggactccattttagatggcaccacacaggg ttgtccactttctctccagtcagctggctgcaggaggagggggtagcaactgggtgctcaagaggctgctggccgtgcccctatggcag tcacatgagctcctttatcagctgagcggccatgggcagacctagcattcaatggccaggagtcaccaggggacaggtggtaaagtggg ggtcacttcatgagacaggagctgtgggtttggggcgctcactgtgccccgagaccaagtcctgttgagacagtgctgactacagagag gcacagaggggtttcaggaacaacccttgcccacccagcaggtccaggtgaggccccacccccctctccctgaatgatggggtgagagt cacctccttccctaaggctgggctcctctccaggtgccgctgagggtggcctgggcggggcagtgagaagggcaggttcgtgcctgcca tggacagggcagggtctatgactggacccagcctgtgcccctcccaagccctactcctgggggctgggggcagcagcaaaaaggagtgg tggagagttcttgtaccactgtgggcacttggccactgctcaccgacgaacgacattttccacagGAGCCGACCTGCCTACAGACCCGC CTGGAGCTGTACAAGCAGGGCCTGCGGGGCAGCCTCACCAAGCTCAAGGGCCCCTTGACCATGATGGCCAGCCACTACAAGCAGCACTG CCCTCCAACCCCGgtgagtgc Right ITR of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 51 AGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGCCCG GGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGCTGCCTGCAGG Complete sequence of vector for insertion of CD34 into GM-CSF locus SEQ ID NO: 3054 CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGC GCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTcctgagatggatgcagccacagccctggagccagcctgaagctcctgg tgtcttctgggggctacatataggagtgtagtccgaacctcagaggggcaaacctgctctgcagagggaatcaaggttcacataaccag agaggggagtcactcaggaaggtggctccagagccaagagtcagactctgggtcccgacttgacccagccacaccccctctgaagcttg ctgagagtggctgcagtctcgctgctggatgtgcacatggtggtcattccctctgctcacaggggcaggggtccccccttactggactg aggttgccccctgctccaggtcctgggtgggagcccatgtgaactgtcagtggggcaggtctgtgagagctcccctcacactcaagtct ctcacagtggccagagaagaggaaggctggagtcagaatgaggcaccagggcgggcatagcctgcccaaaggcccctgggattacaggc aggatggggagccctatctaagtgtctcccacgccccaccccagccattccaggccaggaagtccaaactgtgcccctcagagggaggg ggcagcctcaggcccattcagactgcccagggagggctggagagccctcaggaaggcgggtgggtgggctgtcggttcttggaaaggtt cattaatgaaaacccccaagcctgaccacctagggaaaaggctcaccgttcccatgtgtggctgataagggccaggagattccacagtt caggtagttcccccgcctccctggcattttgtggtcaccattaatcatttcctctgtgtatttaagagctcttttgccagtgagcccaG TACACAGAGAGAAAGGCTAAAGTTCTCTGGAGGATGTGGCTGCAGAGCCTGCTGCTCTTGGGCACTGTGGCCTGCAGCATCTCTGCACC CGCCCGCTCGCCCAGCCCCAGCACGCAGCCCTGGGAGCATGTGAATGCCATCCAGGAGGCCCGGCTCCGGTGCCCGTCAGTGGGCAGAG CGCACATCGCCCACAGTCCCCGAGAAGTTGGGGGGAGGGGTCGGCAATTGATCCGGTGCCTAGAGAAGGTGGCGCGGGGTAAACTGGGA AAGTGATGTCGTGTACTGGCTCCGCCTTTTTCCCGAGGGTGGGGGAGAACCGTATATAAGTGCAGTAGTCGCCGTGAACGTTCTTTTTC GCAACGGGTTTGCCGCCAGAACACAGGatgccgcggggctggaccgcgctttgcttgctgagtttgctgccttctgggttcatgagtct tgacaacaacggtactgctaccccagagttacctacccagggaacattttcaaatgtttctacaaatgtatcctaccaagaaactacaa cacctagtacccttggaagtaccagcctgcaccctgtgtctcaacatggcaatgaggccacaacaaacatcacagaaacgacagtcaaa ttcacatctacctctgtgataacctcagtttatggaaacacaaactcttctgtccagtcacagacctctgtaatcagcacagtgttcac caccccagccaacgtttcaactccagagacaaccttgaagcctagcctgtcacctggaaatgtttcagacctttcaaccactagcacta gccttgcaacatctcccactaaaccctatacatcatcttctcctatcctaagtgacatcaaggcagaaatcaaatgttcaggcatcaga gaagtgaaattgactcagggcatctgcctggagcaaaataagacctccagctgtgcggagtttaagaaggacaggggagagggcctggc ccgagtgctgtgtggggaggagcaggctgatgctgatgctggggcccaggtatgctccctgctccttgcccagtctgaggtgaggcctc agtgtctactgctggtcttggccaacagaacagaaatttccagcaaactccaacttatgaaaaagcaccaatctgacctgaaaaagctg gggatcctagatttcactgagcaagatgttgcaagccaccagagctattcccaaaagaccctgattgcactggtcacctcgggagccct gctggctgtcttgggcatcactggctatttcctgatgaatcgccgcagctggagccccatttaaACGGGTGGCATCCCTGTGACCCCTC CCCAGTGCCTCTCCTGGCCCTGGAAGTTGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAAATTAAGTTGCATCATTTTGTCTGACT AGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTGGTATGGAGCAAGGGGCAAGTTGGGAAGACAACCTGTAGGGCCTGCGGGGTC TATTGGGAACCAAGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCC TCCCGAGTTGTTGGGATTCCAGGCATGCATGACCAGGCTCAGCTAATTTTTGTTTTTTTGGTAGAGACGGGGTTTCACCATATTGGCCA GGCTGGTCTCCAACTCCTAATCTCAGGTGATCTACCCACCTTGGCCTCCCAAATTGCTGGGATTACAGGCGTGAACCACTGCTCCCTTC CCTGTCCTTCTGATTTTGTAGGTAACCACGTGCGGACCGACGTCTCCTGAACCTGAGTAGAGACACTGCTGCTGAGATGgtaagtgaga gaatgtgggcctgtgcctaggccacccagctggcccctgactggccacgcctgtcagcttgataacatgacattttccttttctacagA ATGAAACAGTAGAAGTCATCTCAGAAATGTTTGACCTCCAGgtaagatgcttctctctgacatagctttccagaagcccctgccctggg gtggaggtggggactccattttagatggcaccacacagggttgtccactttctctccagtcagctggctgcaggaggagggggtagcaa ctgggtgctcaagaggctgctggccgtgcccctatggcagtcacatgagctcctttatcagctgagcggccatgggcagacctagcatt caatggccaggagtcaccaggggacaggtggtaaagtgggggtcacttcatgagacaggagctgtgggtttggggcgctcactgtgccc cgagaccaagtcctgttgagacagtgctgactacagagaggcacagaggggtttcaggaacaacccttgcccacccagcaggtccaggt gaggccccacccccctctccctgaatgatggggtgagagtcacctccttccctaaggctgggctcctctccaggtgccgctgagggtgg cctgggcggggcagtgagaagggcaggttcgtgcctgccatggacagggcagggtctatgactggacccagcctgtgcccctcccaagc cctactcctgggggctgggggcagcagcaaaaaggagtggtggagagttcttgtaccactgtgggcacttggccactgctcaccgacga acgacattttccacagGAGCCGACCTGCCTACAGACCCGCCTGGAGCTGTACAAGCAGGGCCTGCGGGGCAGCCTCACCAAGCTCAAGG GCCCCTTGACCATGATGGCCAGCCACTACAAGCAGCACTGCCCTCCAACCCCGgtgagtgcAGGAACCCCTAGTGATGGAGTTGGCCAC TCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGCCCGGGCTTTGCCCGGGCGGCCTCAGTGAGCG AGCGAGCGCGCAGCTGCCTGCAGG left ITR of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3048 CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGC GCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCT cloning remnants of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3055 GCGGCCGCATCGATTGaattc CD3 L homology arm of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3056 AGGTAAGTCCACGAATCAGTGATTCAGTGGTGTGGAGAGCTTTATTTCTGAGAAGGCCAGTAGCGCTCCCTTCTGACAAGCAAATCTAA GACCTGGATGACAGATGACTTCCTGCATTTGGTTGGTTCTTTTGTCATTCATATCTATCTGTAATACAGTTCTGGCTAATTTAAGAGGA TAAGCTTGAAGACCTCTGGAATTTTTCGGCTTTAGGACTTTAAGGCTTTCTGAGCTTCAGTAGATCTAGATCTAGGAGCTCATGCTGGT ATATTCTGAATCCGATGTATCTGAGTTACATCTATGAGCTACTTAATAAATATATCTATGAGCTAAATCTCATAGGCTAAGCATGAACC TCACCTCCAAGACTCGGGGTTCCTAAATGGATGAGACCCTCTTTGGGAAGTCTTGTGGGCAGTGTCTAATTCCACTAGAAAAGTTTTAC CTACAATTTAAACTTAAACCATGATATTTTCTTACTGCTGTTTCCTTTTTTCATTTTCAGGTGGTATTACACAGACACGTGAGTTTATT GGTCTTTTATTTATGCCCTGTCTGAGGATGCAGATTGGTGGGTAGATGAGAAGGAACTGATTGAGAGAGATTAACCCCAAGAACTGATA TCTTCCCAGCATTGCATTCTCAACTCCATTTTAGAAAGGTTCCAAATAGGGACTTCTGTGGGTTTTTCTTTACATCCATCTTACCCTTC CCAAGTCCCCATGTCCCTGCGTAAACCCTAAAGCCACCTCTCAAAAGGTTCTCTAGTTCCCTTCAAGGTTCTCTAGTTCCCTTCATTCC ACATATCTCCTCTTCCACACCCTCTAGCCAGTAGAGCTCCCTTCTGACAAGCAAGTCTAAGATCTAGATGACAGATGACTTCCTGCATT TGGGTGGTTCTTTTGTCACTAATTTGCCTTTTCTAAAATTGTCCTGGTTTCTTCTGCCAATTTCCCTTCTTTCTCCCCAGCATATAAAG TCTCCATCTCTGGAACCACA CAR7 of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3057 atggccttaccagtgaccgccttgctcctgccgctggccttgctgctccacgccgccaggccggatatccagatgacacagactacatc ctccctgtctgcctctctgggagacagagtcaccatcagttgcagtgcaagtcagggcattagcaattatttaaactggtatcagcaga aaccagatggaactgttaaactcctgatctattacacatcaagtttacactcaggagtcccatcaaggttcagtggcagtgggtctggg acagattattctctcaccatcagcaacctggaacctgaagatattgccacttattattgtcagcagtatagcaagcttccgtacacgtt cggaggggggaccaagctggaaataaaacgtggtggtggtggttctggtggtggtggttctggcggcggcggctccggtggtggtggat ccgaggtgcaactggtggagtctgggggaggcttagtgaagcctggggggtccctgaaactctcctgtgcagcctctggactcactttc agtagctatgccatgtcttgggttcgccagactccagagaagaggctggagtgggtcgcatccattagtagtggtggtttcacctacta tccagacagtgtgaagggccgattcaccatctccagagataatgccaggaacatcctgtatctgcaaatgagcagtctgaggtctgagg acacggccatgtattactgtgcaagagacgaggtacgggggtacctcgatgtctggggcgcagggaccacggtcaccgtttcccctagg GCTAGCaccacgacgccagcgccgcgaccaccaacaccggcgcccaccatcgcgtcgcagcccctgtccctgcgcccagaggcgtgccg gccagcggcggggggcgcagtgcacacgagggggctggacttcgcctgtgatttttgggtgctggtggtggttggtggagtcctggctt gctatagcttgctagtaacagtggcctttattattttctgggtgaggagtaagaggagcaggctcctgcacagtgactacatgaacatg actccccgccgccccgggcccacccgcaagcattaccagccctatgccccaccacgcgacttcgcagcctatcgctccagagtgaagtt cagcaggagcgcagacgcccccgcgtacaagcagggccagaaccagctctataacgagctcaatctaggacgaagagaggagtacgatg ttttggacaagagacgtggccgggaccctgagatggggggaaagccgagaaggaagaaccctcaggaaggcctgtacaatgaactgcag aaagataagatggcggaggcctacagtgagattgggatgaaaggcgagcgccggaggggcaaggggcacgatggcctttaccagggtct cagtacagccaccaaggacacctacgacgcccttcacatgcaggccctgccccctcgcCGGACCGATggaagcggagctactaacttca gcctgctgaagcaggctggagacgtggaggagaaccctggacctgtttctgaagccatgccgcggggctggaccgcgctttgcttgctg agtttgctgccttctgggttcatgagtcttgacaacaacggtactgctaccccagagttacctacccagggaacattttcaaatgtttc tacaaatgtatcctaccaagaaactacaacacctagtacccttggaagtaccagcctgcaccctgtgtctcaacatggcaatgaggcca caacaaacatcacagaaacgacagtcaaattcacatctacctctgtgataacctcagtttatggaaacacaaactcttctgtccagtca cagacctctgtaatcagcacagtgttcaccaccccagccaacgtttcaactccagagacaaccttgaagcctagcctgtcacctggaaa tgtttcagacctttcaaccactagcactagccttgcaacatctcccactaaaccctatacatcatcttctcctatcctaagtgacatca aggcagaaatcaaatgttcaggcatcagagaagtgaaattgactcagggcatctgcctggagcaaaataagacctccagctgtgcggag tttaagaaggacaggggagagggcctggcccgagtgctgtgtggggaggagcaggctgatgctgatgctggggcccaggtatgctccct gctccttgcccagtctgaggtgaggcctcagtgtctactgctggtcttggccaacagaacagaaatttccagcaaactccaacttatga aaaagcaccaatctgacctgaaaaagctggggatcctagatttcactgagcaagatgttgcaagccaccagagctattcccaaaagacc ctgattgcactggtcacctcgggagccctgctggctgtcttgggcatcactggctatttcctgatgaatcgccgcagctggagccccat ttaa GFP of donor construct for inserting into CD3ϵ locus SEQ ID NO: 3058 ATGGTGAGCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCATCCTGGTCGAGCTGGACGGCGACGTAAACGGCCACAAGTTCAGCGT GTCCGGCGAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACCCTGAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCA CCCTCGTGACCACCCTGACCTACGGCGTGCAGTGCTTCAGCCGCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATG CCCGAAGGCTACGTCCAGGAGCGCACCATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACAC CCTGGTGAACCGCATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAACAGCC ACAACGTCTATATCATGGCCGACAAGCAGAAGAACGGCATCAAGGTGAACTTCAAGATCCGCCACAACATCGAGGACGGCAGCGTGCAG CTCGCCGACCACTACCAGCAGAACACCCCCATCGGCGACGGCCCCGTGCTGCTGCCCGACAACCACTACCTGAGCACCCAGTCCGCCCT GAGCAAAGACCCCAACGAGAAGCGCGATCACATGGTCCTGCTGGAGTTCGTGACCGCCGCCGGGATCACTCTCGGCATGGACGAGCTGT ACAAGTAA hGMB poly A of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3059 ACGGGTGGCATCCCTGTGACCCCTCCCCAGTGCCTCTCCTGGCCCTGGAAGTTGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAAA TTAAGTTGCATCATTTTGTCTGACTAGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTGGTATGGAGCAAGGGGCAAGTTGGGAA GACAACCTGTAGGGCCTGCGGGGTCTATTGGGAACCAAGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCCGCCTCCTGGG TTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTTGTTGGGATTCCAGGCATGCATGACCAGGCTCAGCTAATTTTTGTTTTTTTGGTAG AGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCCAACTCCTAATCTCAGGTGATCTACCCACCTTGGCCTCCCAAATTGCTGGGATT ACAGGCGTGAACCACTGCTCCCTTCCCTGTCCTTCTGATTTTGTAGGTAACCAC CD3e R homology ARM of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3060 aGTAtaatattgacatgccctcagtatcctggatctgaaatactatggcaacacaatgataaaaacataggcggtgatgaggatgataa aaacataggcagtgatgaggatcacctgtcactgaaggaattttcagaattggagcaaagtggttattatgtctgctaccccagaggaa gcaaaccagaagatgcgaacttttatctctacctgagggcaagagtgtgtgagaactgcatggagatggatgtgatgtcggtggccaca attgtcatagtggacatctgcatcactgggggcttgctgctgctggtttactactggagcaagaatagaaaggccaaggccaagcctgt gacacgaggagcgggtgctggcggcaggcaaaggggacaaaacaaggagaggccaccacctgttcccaacccagactatgagcccatcc ggaaaggccagcgggacctgtattctggcctgaatcagagacgcatctgaccctctggagaacactgcctcccgctggcccaggtctcc tctccagtccccctgcgactccctgtttcctgggctagtcttggaccccacgagagagaatcgttcctcagcctcatggtgaactcgcg ccctccagcctgatcccccgctccctcctccctgccttctctgctggtacccagtcctaaaatattgctgcttcctcttcctttgaagc atcatcagtagtcacaccctcacagctggcctgccctcttgccaggatatttatttgtgctattcactcccttccctttggatgtaact tctccgttcagttccctccttttcttgcatgtaagttgtcccccatcccaaagtattccatctacttttctatcgccgtccccttttgc agccctctctggggatggactgggtaaatgttgacagaggccctgccccgttcacagatcctggccctgagccagccctgtgctcctcc ctcccccaacactccctaccaacc cloning remnants of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3061 GCGgacCGAGCGGCCGC right ITR of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3062 AGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGCCCG GGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGCTGCCTGCAGG cloning remnants of donor construct for inserting GFP into CD3ϵ locus SEQ ID NO: 3063 CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGC GCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTGCGGCCGCATCGATTGaattcAGGTAAGTCCACGAATCAGTGATTCAG TGGTGTGGAGAGCTTTATTTCTGAGAAGGCCAGTAGCGCTCCCTTCTGACAAGCAAATCTAAGACCTGGATGACAGATGACTTCCTGCA TTTGGTTGGTTCTTTTGTCATTCATATCTATCTGTAATACAGTTCTGGCTAATTTAAGAGGATAAGCTTGAAGACCTCTGGAATTTTTC GGCTTTAGGACTTTAAGGCTTTCTGAGCTTCAGTAGATCTAGATCTAGGAGCTCATGCTGGTATATTCTGAATCCGATGTATCTGAGTT ACATCTATGAGCTACTTAATAAATATATCTATGAGCTAAATCTCATAGGCTAAGCATGAACCTCACCTCCAAGACTCGGGGTTCCTAAA TGGATGAGACCCTCTTTGGGAAGTCTTGTGGGCAGTGTCTAATTCCACTAGAAAAGTTTTACCTACAATTTAAACTTAAACCATGATAT TTTCTTACTGCTGTTTCCTTTTTTCATTTTCAGGTGGTATTACACAGACACGTGAGTTTATTGGTCTTTTATTTATGCCCTGTCTGAGG ATGCAGATTGGTGGGTAGATGAGAAGGAACTGATTGAGAGAGATTAACCCCAAGAACTGATATCTTCCCAGCATTGCATTCTCAACTCC ATTTTAGAAAGGTTCCAAATAGGGACTTCTGTGGGTTTTTCTTTACATCCATCTTACCCTTCCCAAGTCCCCATGTCCCTGCGTAAACC CTAAAGCCACCTCTCAAAAGGTTCTCTAGTTCCCTTCAAGGTTCTCTAGTTCCCTTCATTCCACATATCTCCTCTTCCACACCCTCTAG CCAGTAGAGCTCCCTTCTGACAAGCAAGTCTAAGATCTAGATGACAGATGACTTCCTGCATTTGGGTGGTTCTTTTGTCACTAATTTGC CTTTTCTAAAATTGTCCTGGTTTCTTCTGCCAATTTCCCTTCTTTCTCCCCAGCATATAAAGTCTCCATCTCTGGAACCACAATGGTGA GCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCATCCTGGTCGAGCTGGACGGCGACGTAAACGGCCACAAGTTCAGCGTGTCCGGC GAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACCCTGAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCACCCTCGT GACCACCCTGACCTACGGCGTGCAGTGCTTCAGCCGCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATGCCCGAAG GCTACGTCCAGGAGCGCACCATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACACCCTGGTG AACCGCATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAACAGCCACAACGT CTATATCATGGCCGACAAGCAGAAGAACGGCATCAAGGTGAACTTCAAGATCCGCCACAACATCGAGGACGGCAGCGTGCAGCTCGCCG ACCACTACCAGCAGAACACCCCCATCGGCGACGGCCCCGTGCTGCTGCCCGACAACCACTACCTGAGCACCCAGTCCGCCCTGAGCAAA GACCCCAACGAGAAGCGCGATCACATGGTCCTGCTGGAGTTCGTGACCGCCGCCGGGATCACTCTCGGCATGGACGAGCTGTACAAGTA AACGGGTGGCATCCCTGTGACCCCTCCCCAGTGCCTCTCCTGGCCCTGGAAGTTGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAA ATTAAGTTGCATCATTTTGTCTGACTAGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTGGTATGGAGCAAGGGGCAAGTTGGGA AGACAACCTGTAGGGCCTGCGGGGTCTATTGGGAACCAAGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCCGCCTCCTGG GTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTTGTTGGGATTCCAGGCATGCATGACCAGGCTCAGCTAATTTTTGTTTTTTTGGTA GAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCCAACTCCTAATCTCAGGTGATCTACCCACCTTGGCCTCCCAAATTGCTGGGAT TACAGGCGTGAACCACTGCTCCCTTCCCTGTCCTTCTGATTTTGTAGGTAACCACaGTAtaatattgacatgccctcagtatcctggat ctgaaatactatggcaacacaatgataaaaacataggcggtgatgaggatgataaaaacataggcagtgatgaggatcacctgtcactg aaggaattttcagaattggagcaaagtggttattatgtctgctaccccagaggaagcaaaccagaagatgcgaacttttatctctacct gagggcaagagtgtgtgagaactgcatggagatggatgtgatgtcggtggccacaattgtcatagtggacatctgcatcactgggggct tgctgctgctggtttactactggagcaagaatagaaaggccaaggccaagcctgtgacacgaggagcgggtgctggcggcaggcaaagg ggacaaaacaaggagaggccaccacctgttcccaacccagactatgagcccatccggaaaggccagcgggacctgtattctggcctgaa tcagagacgcatctgaccctctggagaacactgcctcccgctggcccaggtctcctctccagtccccctgcgactccctgtttcctggg ctagtcttggaccccacgagagagaatcgttcctcagcctcatggtgaactcgcgccctccagcctgatcccccgctccctcctccctg ccttctctgctggtacccagtcctaaaatattgctgcttcctcttcctttgaagcatcatcagtagtcacaccctcacagctggcctgc cctcttgccaggatatttatttgtgctattcactcccttccctttggatgtaacttctccgttcagttccctccttttcttgcatgtaa gttgtcccccatcccaaagtattccatctacttttctatcgccgtccccttttgcagccctctctggggatggactgggtaaatgttga cagaggccctgccccgttcacagatcctggccctgagccagccctgtgctcctccctcccccaacactccctaccaaccGCGgacCGAG CGGCCGCAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCG ACGCCCGGGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGCTGCCTGCAGG complete sequence of vector for insertion of GFP into CD3ϵ locus SEQ ID NO: 3064 CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGC GCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTGCGGCCGCATCGATTGaattcAGGTAAGTCCACGAATCAGTGATTCAG TGGTGTGGAGAGCTTTATTTCTGAGAAGGCCAGTAGCGCTCCCTTCTGACAAGCAAATCTAAGACCTGGATGACAGATGACTTCCTGCA TTTGGTTGGTTCTTTTGTCATTCATATCTATCTGTAATACAGTTCTGGCTAATTTAAGAGGATAAGCTTGAAGACCTCTGGAATTTTTC GGCTTTAGGACTTTAAGGCTTTCTGAGCTTCAGTAGATCTAGATCTAGGAGCTCATGCTGGTATATTCTGAATCCGATGTATCTGAGTT ACATCTATGAGCTACTTAATAAATATATCTATGAGCTAAATCTCATAGGCTAAGCATGAACCTCACCTCCAAGACTCGGGGTTCCTAAA TGGATGAGACCCTCTTTGGGAAGTCTTGTGGGCAGTGTCTAATTCCACTAGAAAAGTTTTACCTACAATTTAAACTTAAACCATGATAT TTTCTTACTGCTGTTTCCTTTTTTCATTTTCAGGTGGTATTACACAGACACGTGAGTTTATTGGTCTTTTATTTATGCCCTGTCTGAGG ATGCAGATTGGTGGGTAGATGAGAAGGAACTGATTGAGAGAGATTAACCCCAAGAACTGATATCTTCCCAGCATTGCATTCTCAACTCC ATTTTAGAAAGGTTCCAAATAGGGACTTCTGTGGGTTTTTCTTTACATCCATCTTACCCTTCCCAAGTCCCCATGTCCCTGCGTAAACC CTAAAGCCACCTCTCAAAAGGTTCTCTAGTTCCCTTCAAGGTTCTCTAGTTCCCTTCATTCCACATATCTCCTCTTCCACACCCTCTAG CCAGTAGAGCTCCCTTCTGACAAGCAAGTCTAAGATCTAGATGACAGATGACTTCCTGCATTTGGGTGGTTCTTTTGTCACTAATTTGC CTTTTCTAAAATTGTCCTGGTTTCTTCTGCCAATTTCCCTTCTTTCTCCCCAGCATATAAAGTCTCCATCTCTGGAACCACAatggcct taccagtgaccgccttgctcctgccgctggccttgctgctccacgccgccaggccggatatccagatgacacagactacatcctccctg tctgcctctctgggagacagagtcaccatcagttgcagtgcaagtcagggcattagcaattatttaaactggtatcagcagaaaccaga tggaactgttaaactcctgatctattacacatcaagtttacactcaggagtcccatcaaggttcagtggcagtgggtctgggacagatt attctctcaccatcagcaacctggaacctgaagatattgccacttattattgtcagcagtatagcaagcttccgtacacgttcggaggg gggaccaagctggaaataaaacgtggtggtggtggttctggtggtggtggttctggcggcggcggctccggtggtggtggatccgaggt gcaactggtggagtctgggggaggcttagtgaagcctggggggtccctgaaactctcctgtgcagcctctggactcactttcagtagct atgccatgtcttgggttcgccagactccagagaagaggctggagtgggtcgcatccattagtagtggtggtttcacctactatccagac agtgtgaagggccgattcaccatctccagagataatgccaggaacatcctgtatctgcaaatgagcagtctgaggtctgaggacacggc catgtattactgtgcaagagacgaggtacgggggtacctcgatgtctggggcgcagggaccacggtcaccgtttcccctaggGCTAGCa ccacgacgccagcgccgcgaccaccaacaccggcgcccaccatcgcgtcgcagcccctgtccctgcgcccagaggcgtgccggccagcg gcggggggcgcagtgcacacgagggggctggacttcgcctgtgatttttgggtgctggtggtggttggtggagtcctggcttgctatag cttgctagtaacagtggcctttattattttctgggtgaggagtaagaggagcaggctcctgcacagtgactacatgaacatgactcccc gccgccccgggcccacccgcaagcattaccagccctatgccccaccacgcgacttcgcagcctatcgctccagagtgaagttcagcagg agcgcagacgcccccgcgtacaagcagggccagaaccagctctataacgagctcaatctaggacgaagagaggagtacgatgttttgga caagagacgtggccgggaccctgagatggggggaaagccgagaaggaagaaccctcaggaaggcctgtacaatgaactgcagaaagata agatggcggaggcctacagtgagattgggatgaaaggcgagcgccggaggggcaaggggcacgatggcctttaccagggtctcagtaca gccaccaaggacacctacgacgcccttcacatgcaggccctgccccctcgcCGGACCGATggaagcggagctactaacttcagcctgct gaagcaggctggagacgtggaggagaaccctggacctgtttctgaagccatgccgcggggctggaccgcgctttgcttgctgagtttgc tgccttctgggttcatgagtcttgacaacaacggtactgctaccccagagttacctacccagggaacattttcaaatgtttctacaaat gtatcctaccaagaaactacaacacctagtacccttggaagtaccagcctgcaccctgtgtctcaacatggcaatgaggccacaacaaa catcacagaaacgacagtcaaattcacatctacctctgtgataacctcagtttatggaaacacaaactcttctgtccagtcacagacct ctgtaatcagcacagtgttcaccaccccagccaacgtttcaactccagagacaaccttgaagcctagcctgtcacctggaaatgtttca gacctttcaaccactagcactagccttgcaacatctcccactaaaccctatacatcatcttctcctatcctaagtgacatcaaggcaga aatcaaatgttcaggcatcagagaagtgaaattgactcagggcatctgcctggagcaaaataagacctccagctgtgcggagtttaaga aggacaggggagagggcctggcccgagtgctgtgtggggaggagcaggctgatgctgatgctggggcccaggtatgctccctgctcctt gcccagtctgaggtgaggcctcagtgtctactgctggtcttggccaacagaacagaaatttccagcaaactccaacttatgaaaaagca ccaatctgacctgaaaaagctggggatcctagatttcactgagcaagatgttgcaagccaccagagctattcccaaaagaccctgattg cactggtcacctcgggagccctgctggctgtcttgggcatcactggctatttcctgatgaatcgccgcagctggagccccatttaaACG GGTGGCATCCCTGTGACCCCTCCCCAGTGCCTCTCCTGGCCCTGGAAGTTGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAAATTA AGTTGCATCATTTTGTCTGACTAGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTGGTATGGAGCAAGGGGCAAGTTGGGAAGAC AACCTGTAGGGCCTGCGGGGTCTATTGGGAACCAAGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCCGCCTCCTGGGTTC AAGCGATTCTCCTGCCTCAGCCTCCCGAGTTGTTGGGATTCCAGGCATGCATGACCAGGCTCAGCTAATTTTTGTTTTTTTGGTAGAGA CGGGGTTTCACCATATTGGCCAGGCTGGTCTCCAACTCCTAATCTCAGGTGATCTACCCACCTTGGCCTCCCAAATTGCTGGGATTACA GGCGTGAACCACTGCTCCCTTCCCTGTCCTTCTGATTTTGTAGGTAACCACaGTAtaatattgacatgccctcagtatcctggatctga aatactatggcaacacaatgataaaaacataggcggtgatgaggatgataaaaacataggcagtgatgaggatcacctgtcactgaagg aattttcagaattggagcaaagtggttattatgtctgctaccccagaggaagcaaaccagaagatgcgaacttttatctctacctgagg gcaagagtgtgtgagaactgcatggagatggatgtgatgtcggtggccacaattgtcatagtggacatctgcatcactgggggcttgct gctgctggtttactactggagcaagaatagaaaggccaaggccaagcctgtgacacgaggagcgggtgctggcggcaggcaaaggggac aaaacaaggagaggccaccacctgttcccaacccagactatgagcccatccggaaaggccagcgggacctgtattctggcctgaatcag agacgcatctgaccctctggagaacactgcctcccgctggcccaggtctcctctccagtccccctgcgactccctgtttcctgggctag tcttggaccccacgagagagaatcgttcctcagcctcatggtgaactcgcgccctccagcctgatcccccgctccctcctccctgcctt ctctgctggtacccagtcctaaaatattgctgcttcctcttcctttgaagcatcatcagtagtcacaccctcacagctggcctgccctc ttgccaggatatttatttgtgctattcactcccttccctttggatgtaacttctccgttcagttccctccttttcttgcatgtaagttg tcccccatcccaaagtattccatctacttttctatcgccgtccccttttgcagccctctctggggatggactgggtaaatgttgacaga ggccctgccccgttcacagatcctggccctgagccagccctgtgctcctccctcccccaacactccctaccaaccGCGgacCGAGCGGC CGCAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGC CCGGGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGCTGCCTGCAGG

All references, patents or applications, U.S. or foreign, cited in the application are hereby incorporated by reference as if written herein in their entireties. Where any inconsistencies arise, material literally disclosed herein controls.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modification of the invention to adapt it to various usages and conditions.

E 0.172 0.17 0.073 0.075 0.085 0.084 0.492 0.557 0.42 0.18 0.247 0.19 450 (Test) 0.046 0.045 0.044 0.046 0.045 0.045 0.05 0.053 0.05 0.048 0.048 0.047 540 (Ref) 0.698 0.691 0.161 0.161 0.222 0.216 2.46 2.796 2.054 0.735 1.107 0.794 Pathlength 0.171 0.17 0.073 0.075 0.085 0.084 0.496 0.558 0.42 0.181 0.249 0.19 450 0.046 0.046 0.045 0.047 0.045 0.045 0.05 0.053 0.051 0.048 0.049 0.047 540 0.245 0.246 0.454 0.468 0.383 0.389 0.202 0.2 0.204 0.246 0.225 0.239 Corrected [450] 0.066 0.066 0.277 0.291 0.204 0.209 0.02 0.019 0.025 0.066 0.044 0.059 Corrected [540] F 0.127 0.124 0.07 0.074 0.075 0.072 0.148 0.143 0.128 0.102 0.115 0.121 450 (Test) 0.044 0.045 0.043 0.047 0.046 0.044 0.055 0.057 0.045 0.045 0.051 0.048 540 (Ref) 0.458 0.436 0.147 0.15 0.162 0.157 0.516 0.479 0.463 0.316 0.353 0.406 Pathlength 0.127 0.124 0.07 0.074 0.075 0.072 0.147 0.144 0.129 0.102 0.116 0.12 450 0.045 0.045 0.044 0.047 0.046 0.044 0.055 0.057 0.045 0.045 0.052 0.048 540 0.277 0.283 0.475 0.493 0.465 0.462 0.286 0.3 0.278 0.323 0.328 0.296 Corrected [450] 0.097 0.104 0.297 0.314 0.285 0.283 0.106 0.119 0.097 0.144 0.147 0.119 Corrected [540] G 0.098 0.1 0.078 0.073 0.104 0.122 0.143 0.169 0.144 0.125 0.134 0.131 450 (Test) 0.044 0.044 0.046 0.044 0.045 0.05 0.049 0.049 0.05 0.05 0.045 0.046 540 (Ref) 0.301 0.313 0.179 0.161 0.326 0.398 0.523 0.667 0.523 0.415 0.493 0.469 Pathlength 0.099 0.101 0.078 0.073 0.103 0.122 0.144 0.169 0.144 0.125 0.133 0.13 450 0.044 0.044 0.046 0.044 0.045 0.05 0.05 0.049 0.05 0.05 0.045 0.045 540 0.328 0.322 0.437 0.452 0.317 0.306 0.275 0.254 0.275 0.301 0.269 0.277 Corrected [450] 0.148 0.142 0.259 0.272 0.138 0.127 0.095 0.074 0.096 0.12 0.091 0.096 Corrected [540] H 0.082 0.087 0.113 0.12 0.074 0.081 0.165 0.169 0.15 0.103 0.122 0.119 450 (Test) 0.047 0.051 0.049 0.047 0.047 0.053 0.059 0.059 0.045 0.044 0.046 0.044 540 (Ref) 0.197 0.197 0.356 0.406 0.15 0.157 0.611 0.607 0.579 0.329 0.422 0.412 Pathlength 0.082 0.087 0.113 0.12 0.074 0.081 0.165 0.169 0.15 0.103 0.122 0.118 450 0.047 0.052 0.049 0.047 0.047 0.053 0.055 0.06 0.046 0.044 0.046 0.045 540 0.415 0.443 0.316 0.296 0.493 0.516 0.27 0.279 0.259 0.314 0.289 0.288 Corrected [450] 0.236 0.263 0.137 0.117 0.311 0.338 0.09 0.098 0.079 0.134 0.11 0.109 Corrected [540] 

1. A chimeric antigen receptor (CAR)-bearing immune effector cell that is deficient in a cytokine or in a chemokine or in a transcription factor that is involved in cytokine release syndrome.
 2. The cell as recited in claim 1, wherein the cytokine or chemokine or transcription factor deficiency is effected by deletion or suppression of a gene encoding the cytokine or chemokine or transcription factor, or by suppression of a gene transcript of the cytokine or chemokine or transcription factor gene.
 3. The cell as recited in claim 2, wherein the deletion or suppression of the gene encoding the cytokine or chemokine or transcription factor is effected by inserting the CAR into a locus of the cytokine or chemokine or transcription factor gene, or wherein the suppression of the gene transcript of the cytokine or chemokine or transcription factor is effected by transfection of one or more types of small interfering RNAs (siRNA) or by transduction of one or more types of short hairpin RNAs (shRNA).
 4. The cell as recited in claim 3, wherein the CAR is part of a construct that also includes a selectable marker chosen from a green fluorescence (GFP) gene, a YFP gene, a tCD34 gene, or a tEGFR gene. 5.-6. (canceled)
 7. The cell as recited in claim 1, wherein deletion or suppression is effected using CRISPR, Cas9-CRISPR, Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), or Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR).
 8. (canceled)
 9. The cell as recited in claim 7, wherein the Cas9 is delivered into the cell as mRNA or protein, and/or wherein a guide RNA (gRNA) targeting the gene to be deleted or suppressed is delivered contemporaneously with the Cas9. 10.-15. (canceled)
 16. The cell of claim 2, wherein: the cell expresses at least one CAR that is inserted into a locus of the gene encoding the cytokine or chemokine or transcription factor; the gene encoding the cytokine or chemokine or transcription factor is deleted or suppressed by a method chosen from Transcription Activator-like Effector Nucleases (TALENs), Zinc Finger Nucleases (ZFNs), and Clustered Regularly Interspaces Short Palindromic Repeats (CRISPR) editing; the cytokine or chemokine or transcription factor is suppressed by expression of an scFv with an endoplasmic reticulum (ER) binding tether to bind the cytokine or chemokine in the ER and prevent secretion; the cytokine or chemokine or transcription factor gene transcript is suppressed by transfection of small interfering RNAs (siRNAs); the cytokine or chemokine or transcription factor gene transcript is suppressed by transduction of short hairpin RNAs (shRNAs); the gene that is deleted or suppressed is a T cell surface receptor that is integrated into CAR-T cell signaling.
 17. The cell as recited in claim 1, wherein the cell is chosen from a chimeric antigen receptor T cell (CAR-T), a CAR-bearing iNKT cell (iNKT-CAR), and a CAR-bearing natural killer (NK) cell (NK-CAR), or a CAR-bearing macrophage.
 18. (canceled)
 19. The cell as recited in claim 17, wherein the cell is a dual or tandem CAR-T or iNKT-CAR or CAR-bearing macrophage. 20.-23. (canceled)
 24. The cell as recited in claim 1, wherein the cytokine or chemokine or transcription factor contributes to the development of cytokine release syndrome and is selected from among those recited in Table
 10. 25. (canceled)
 26. The cell as recited in claim 24, wherein the cytokine or chemokine or transcription factor is produced by T cells that activate or localize myeloid cells, or is a T cell surface receptor gene that activates myeloid or CAR-T cells. 27.-28. (canceled)
 29. The cell as recited in claim 1, wherein the cytokine or chemokine or transcription factor drives T cell/CAR-T cell differentiation, or wherein the cytokine or chemokine is a transcription factor that drives T cell/CAT-T cell differentiation.
 30. (canceled)
 31. The cell as recited in claim 1, wherein the cytokine or chemokine or transcription factor is chosen from MCP1 (CCL2), MCP-2, GM-CSF, G-CSF, M-CSF, Il-4, and IFNγ.
 32. (canceled)
 33. The cell as recited in claim 31, wherein the cell is a GM-CSF deficient CAR-T cell or a GM-CSF deficient iNKT-CAR cell. 34.-36. (canceled)
 37. The cell as recited in claim 1, wherein the chimeric antigen receptor(s) specifically binds at least one antigen expressed on a malignant cell, a malignant T cell, a malignant B cell, a malignant mesothelial cell, or a malignant plasma cell.
 38. The cell as recited in claim 37, wherein the at least one antigen expressed on a malignant cell is chosen from BCMA, CS1, CD38, CD138, CD19, CD33, CD123, CD371, CD117, CD135, Tim-3, CD5, CD7, CD2, CD4, CD3, CD79A, CD79B, APRIL, CD56, and CD1a; or wherein the at least one antigen expressed on a malignant T cell is chosen from CD2, CD3ε, CD4, CD5, CD7, TCRA, and TCRβ; or wherein the at least one antigen expressed on a malignant B cell is chosen from CD19, CD20, CD21, CD22, CD23, CD24, CD25, CD27, CD38, and CD45; or wherein the at least one antigen expressed on a malignant mesothelial cell is mesothelin; or wherein the at least one antigen expressed on a malignant plasma cell is chosen from BCMA, CS1, CD38, and CD19. 39.-47. (canceled)
 48. The cell as recited in claim 37, wherein the chimeric antigen receptor expresses the extracellular portion of the APRIL protein, the ligand for BCMA and TACI, effectively co-targeting both BCMA and TACI.
 49. (canceled)
 50. The cell as recited in claim 1, wherein endogenous T cell receptor mediated signaling is negligible in the cell.
 51. The cell as recited in claim 50, wherein the cell does not induce alloreactivity, graft-versus-host disease, or fratricide.
 52. (canceled)
 53. A method of treatment of cancer in a patient, which has a reduced incidence of cytokine release syndrome and/or CAR-T associated neuropathy, comprising the administration of cells as recited in claim
 1. 54. The method as recited in claim 53, wherein the cancer is a hematologic malignancy chosen from a T-cell malignancy, multiple myeloma, or acute myeloid leukemia (AML), or a solid tumor chosen from cervical cancer, pancreatic cancer, ovarian cancer, mesothelioma, or lung cancer. 55.-94. (canceled) 